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nsv10097

  • Variant Calls:11
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59,912

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 409 SVs from 33 studies. See in: genome view    
Remapped(Score: Good):97,192,026-97,251,937Question Mark
Overlapping variant regions from other studies: 409 SVs from 33 studies. See in: genome view    
Remapped(Score: Good):97,857,763-97,917,674Question Mark
Submitted genomic97,279,637-97,339,539Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv10097RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr297,192,02697,251,937
nsv10097RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr297,857,76397,917,674
nsv10097Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000002.9Chr297,279,63797,339,539

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv27406copy number lossNA18572Oligo aCGHProbe signal intensity483
nssv27618copy number lossNA12740Oligo aCGHProbe signal intensity572
nssv25968copy number lossNA19144Oligo aCGHProbe signal intensity629
nssv27841copy number lossNA18975Oligo aCGHProbe signal intensity529
nssv27843copy number lossNA19007Oligo aCGHProbe signal intensity581
nssv27998copy number lossNA07048Oligo aCGHProbe signal intensity564
nssv25965copy number lossNA18980Oligo aCGHProbe signal intensity561
nssv28083copy number gainNA07048Oligo aCGHProbe signal intensity564
nssv27611copy number gainNA07029Oligo aCGHProbe signal intensity544
nssv29081copy number gainNA18517Oligo aCGHProbe signal intensity698
nssv27726copy number gainNA12740Oligo aCGHProbe signal intensity572

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv27406RemappedGoodNC_000002.12:g.(97
192026_97192026)_(
97233824_97233824)
del		GRCh38.p12First PassNC_000002.12Chr297,192,02697,192,02697,233,82497,233,824
nssv27618RemappedPerfectNC_000002.12:g.(97
193473_97193480)_(
97210299_97210936)
del		GRCh38.p12First PassNC_000002.12Chr297,193,47397,193,48097,210,29997,210,936
nssv25968RemappedPerfectNC_000002.12:g.(97
193480_97193886)_(
97209774_97210299)
del		GRCh38.p12First PassNC_000002.12Chr297,193,48097,193,88697,209,77497,210,299
nssv27841RemappedPerfectNC_000002.12:g.(97
193480_97193886)_(
97209774_97210299)
del		GRCh38.p12First PassNC_000002.12Chr297,193,48097,193,88697,209,77497,210,299
nssv27843RemappedPerfectNC_000002.12:g.(97
193480_97193886)_(
97209774_97210299)
del		GRCh38.p12First PassNC_000002.12Chr297,193,48097,193,88697,209,77497,210,299
nssv27998RemappedPerfectNC_000002.12:g.(97
193480_97193886)_(
97209774_97210299)
del		GRCh38.p12First PassNC_000002.12Chr297,193,48097,193,88697,209,77497,210,299
nssv25965RemappedGoodNC_000002.12:g.(97
193480_97193480)_(
97241502_97241502)
del		GRCh38.p12First PassNC_000002.12Chr297,193,48097,193,48097,241,50297,241,502
nssv28083RemappedGoodNC_000002.12:g.(97
233824_97233824)_(
97251937_97251937)
dup		GRCh38.p12First PassNC_000002.12Chr297,233,82497,233,82497,251,93797,251,937
nssv27611RemappedGoodNC_000002.12:g.(97
241335_97241335)_(
97251182_97251182)
dup		GRCh38.p12First PassNC_000002.12Chr297,241,33597,241,33597,251,18297,251,182
nssv29081RemappedGoodNC_000002.12:g.(97
241335_97241335)_(
97251937_97251937)
dup		GRCh38.p12First PassNC_000002.12Chr297,241,33597,241,33597,251,93797,251,937
nssv27726RemappedPerfectNC_000002.12:g.(97
246012_97246654)_(
97246655_97247151)
dup		GRCh38.p12First PassNC_000002.12Chr297,246,01297,246,65497,246,65597,247,151
nssv27406RemappedGoodNC_000002.11:g.(97
857763_97857763)_(
97899561_97899561)
del		GRCh37.p13First PassNC_000002.11Chr297,857,76397,857,76397,899,56197,899,561
nssv27618RemappedPerfectNC_000002.11:g.(97
859210_97859217)_(
97876036_97876673)
del		GRCh37.p13First PassNC_000002.11Chr297,859,21097,859,21797,876,03697,876,673
nssv25968RemappedPerfectNC_000002.11:g.(97
859217_97859623)_(
97875511_97876036)
del		GRCh37.p13First PassNC_000002.11Chr297,859,21797,859,62397,875,51197,876,036
nssv27841RemappedPerfectNC_000002.11:g.(97
859217_97859623)_(
97875511_97876036)
del		GRCh37.p13First PassNC_000002.11Chr297,859,21797,859,62397,875,51197,876,036
nssv27843RemappedPerfectNC_000002.11:g.(97
859217_97859623)_(
97875511_97876036)
del		GRCh37.p13First PassNC_000002.11Chr297,859,21797,859,62397,875,51197,876,036
nssv27998RemappedPerfectNC_000002.11:g.(97
859217_97859623)_(
97875511_97876036)
del		GRCh37.p13First PassNC_000002.11Chr297,859,21797,859,62397,875,51197,876,036
nssv25965RemappedGoodNC_000002.11:g.(97
859217_97859217)_(
97907239_97907239)
del		GRCh37.p13First PassNC_000002.11Chr297,859,21797,859,21797,907,23997,907,239
nssv28083RemappedGoodNC_000002.11:g.(97
899561_97899561)_(
97917674_97917674)
dup		GRCh37.p13First PassNC_000002.11Chr297,899,56197,899,56197,917,67497,917,674
nssv27611RemappedGoodNC_000002.11:g.(97
907072_97907072)_(
97916919_97916919)
dup		GRCh37.p13First PassNC_000002.11Chr297,907,07297,907,07297,916,91997,916,919
nssv29081RemappedGoodNC_000002.11:g.(97
907072_97907072)_(
97917674_97917674)
dup		GRCh37.p13First PassNC_000002.11Chr297,907,07297,907,07297,917,67497,917,674
nssv27726RemappedPerfectNC_000002.11:g.(97
911749_97912391)_(
97912392_97912888)
dup		GRCh37.p13First PassNC_000002.11Chr297,911,74997,912,39197,912,39297,912,888
nssv27406Submitted genomicNC_000002.9:g.(972
79637_97281084)_(9
7321388_97321432)d
el		NCBI35 (hg17)NC_000002.9Chr297,279,63797,281,08497,321,38897,321,432
nssv27618Submitted genomicNC_000002.9:g.(972
81084_97281091)_(9
7297910_97298547)d
el		NCBI35 (hg17)NC_000002.9Chr297,281,08497,281,09197,297,91097,298,547
nssv25968Submitted genomicNC_000002.9:g.(972
81091_97281497)_(9
7297385_97297910)d
el		NCBI35 (hg17)NC_000002.9Chr297,281,09197,281,49797,297,38597,297,910
nssv27841Submitted genomicNC_000002.9:g.(972
81091_97281497)_(9
7297385_97297910)d
el		NCBI35 (hg17)NC_000002.9Chr297,281,09197,281,49797,297,38597,297,910
nssv27843Submitted genomicNC_000002.9:g.(972
81091_97281497)_(9
7297385_97297910)d
el		NCBI35 (hg17)NC_000002.9Chr297,281,09197,281,49797,297,38597,297,910
nssv27998Submitted genomicNC_000002.9:g.(972
81091_97281497)_(9
7297385_97297910)d
el		NCBI35 (hg17)NC_000002.9Chr297,281,09197,281,49797,297,38597,297,910
nssv25965Submitted genomicNC_000002.9:g.(972
81091_97281497)_(9
7328936_97329103)d
el		NCBI35 (hg17)NC_000002.9Chr297,281,09197,281,49797,328,93697,329,103
nssv28083Submitted genomicNC_000002.9:g.(973
21432_97328936)_(9
7338784_97339539)d
up		NCBI35 (hg17)NC_000002.9Chr297,321,43297,328,93697,338,78497,339,539
nssv27611Submitted genomicNC_000002.9:g.(973
28936_97329103)_(9
7338574_97338784)d
up		NCBI35 (hg17)NC_000002.9Chr297,328,93697,329,10397,338,57497,338,784
nssv29081Submitted genomicNC_000002.9:g.(973
28936_97329103)_(9
7338784_97339539)d
up		NCBI35 (hg17)NC_000002.9Chr297,328,93697,329,10397,338,78497,339,539
nssv27726Submitted genomicNC_000002.9:g.(973
33614_97334256)_(9
7334257_97334753)d
up		NCBI35 (hg17)NC_000002.9Chr297,333,61497,334,25697,334,25797,334,753

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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