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nsv469855

  • Variant Calls:19
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133,881

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2467 SVs from 107 studies. See in: genome view    
Remapped(Score: Perfect):19,902,981-20,036,861Question Mark
Overlapping variant regions from other studies: 2556 SVs from 107 studies. See in: genome view    
Remapped(Score: Perfect):20,371,140-20,505,020Question Mark
Overlapping variant regions from other studies: 2 SVs from 1 studies. See in: genome view    
Submitted genomic18,361,268-18,495,148Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv469855RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1419,902,98120,036,861
nsv469855RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1420,371,14020,505,020
nsv469855Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000014.6Chr1418,361,26818,495,148

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1672512copy number lossBAC aCGHProbe signal intensity
nssv1672571copy number lossBAC aCGHProbe signal intensity
nssv1672615copy number lossBAC aCGHProbe signal intensity
nssv1672768copy number lossBAC aCGHProbe signal intensity
nssv1672781copy number lossBAC aCGHProbe signal intensity
nssv1672904copy number lossBAC aCGHProbe signal intensity
nssv1673092copy number lossBAC aCGHProbe signal intensity
nssv1673202copy number lossBAC aCGHProbe signal intensity
nssv1673373copy number lossBAC aCGHProbe signal intensity
nssv1673786copy number lossBAC aCGHProbe signal intensity
nssv1673799copy number lossBAC aCGHProbe signal intensity
nssv1674226copy number lossBAC aCGHProbe signal intensity
nssv1674570copy number lossBAC aCGHProbe signal intensity
nssv1674686copy number lossBAC aCGHProbe signal intensity
nssv1675161copy number lossBAC aCGHProbe signal intensity
nssv1676210copy number lossBAC aCGHProbe signal intensity
nssv1676225copy number lossBAC aCGHProbe signal intensity
nssv1676544copy number lossBAC aCGHProbe signal intensity
nssv1676716copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1672512RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1672571RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1672615RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1672768RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1672781RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1672904RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1673092RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1673202RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1673373RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1673786RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1673799RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1674226RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1674570RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1674686RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1675161RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1676210RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1676225RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1676544RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1676716RemappedPerfectNC_000014.9:g.(?_1
9902981)_(20036861
_?)del
GRCh38.p12First PassNC_000014.9Chr1419,902,98120,036,861
nssv1672512RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1672571RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1672615RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1672768RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1672781RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1672904RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1673092RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1673202RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1673373RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1673786RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1673799RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1674226RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1674570RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1674686RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1675161RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1676210RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1676225RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1676544RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1676716RemappedPerfectNC_000014.8:g.(?_2
0371140)_(20505020
_?)del
GRCh37.p13First PassNC_000014.8Chr1420,371,14020,505,020
nssv1672512Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1672571Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1672615Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1672768Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1672781Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1672904Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1673092Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1673202Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1673373Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1673786Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1673799Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1674226Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1674570Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1674686Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1675161Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1676210Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1676225Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1676544Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148
nssv1676716Submitted genomicNC_000014.6:g.(?_1
8361268)_(18495148
_?)del
NCBI34 (hg16)NC_000014.6Chr1418,361,26818,495,148

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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