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nsv822039

  • Variant Calls:14
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,382

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 176 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):24,989,428-24,990,809Question Mark
Overlapping variant regions from other studies: 176 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):25,030,919-25,032,300Question Mark
Overlapping variant regions from other studies: 64 SVs from 19 studies. See in: genome view    
Submitted genomic25,005,923-25,007,304Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv822039RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr324,989,42824,990,809
nsv822039RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr325,030,91925,032,300
nsv822039Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr325,005,92325,007,304

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1424872copy number lossAK2Oligo aCGHProbe signal intensity614
nssv1425200copy number gainNA18947Oligo aCGHProbe signal intensity653
nssv1426507copy number lossNA18592Oligo aCGHProbe signal intensity636
nssv1426532copy number lossAK6Oligo aCGHProbe signal intensity714
nssv1429688copy number lossAK14Oligo aCGHProbe signal intensity630
nssv1431203copy number lossAK18Oligo aCGHProbe signal intensity628
nssv1431940copy number lossAK20Oligo aCGHProbe signal intensity768
nssv1432722copy number gainNA18972Oligo aCGHProbe signal intensity750
nssv1434981copy number lossNA18942Oligo aCGHProbe signal intensity712
nssv1435766copy number lossNA18566Oligo aCGHProbe signal intensity605
nssv1436480copy number lossNA18542Oligo aCGHProbe signal intensity805
nssv1438716copy number lossNA18973Oligo aCGHProbe signal intensity782
nssv1439580copy number lossNA18537Oligo aCGHProbe signal intensity597
nssv1440953copy number gainNA18969Oligo aCGHProbe signal intensity898

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1424872RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1425200RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)dup
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1426507RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1426532RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1429688RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1431203RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1431940RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1432722RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)dup
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1434981RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1435766RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1436480RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1438716RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1439580RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)del
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1440953RemappedPerfectNC_000003.12:g.(?_
24989428)_(2499080
9_?)dup
GRCh38.p12First PassNC_000003.12Chr324,989,42824,990,809
nssv1424872RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1425200RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)dup
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1426507RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1426532RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1429688RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1431203RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1431940RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1432722RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)dup
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1434981RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1435766RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1436480RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1438716RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1439580RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)del
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1440953RemappedPerfectNC_000003.11:g.(?_
25030919)_(2503230
0_?)dup
GRCh37.p13First PassNC_000003.11Chr325,030,91925,032,300
nssv1424872Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1425200Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)dup
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1426507Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1426532Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1429688Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1431203Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1431940Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1432722Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)dup
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1434981Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1435766Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1436480Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1438716Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1439580Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)del
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304
nssv1440953Submitted genomicNC_000003.10:g.(?_
25005923)_(2500730
4_?)dup
NCBI36 (hg18)NC_000003.10Chr325,005,92325,007,304

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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