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nsv3169850

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:122,787

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1326 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):134,483,002-134,605,788Question Mark
Overlapping variant regions from other studies: 1326 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):134,352,896-134,475,682Question Mark
Overlapping variant regions from other studies: 547 SVs from 26 studies. See in: genome view    
Submitted genomic133,858,106-133,980,892Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv3169850RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr11134,483,002134,486,015134,602,316134,605,788
nsv3169850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11134,352,896134,355,909134,472,210134,475,682
nsv3169850Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr11133,858,106133,861,119133,977,420133,980,892

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv14244950deletionNGO_18SNP arraySNP genotyping analysis1119
nssv14249888deletionMLY_9SNP arraySNP genotyping analysis0142

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv14244950RemappedPerfectNC_000011.10:g.(13
4483002_134486015)
_(134596762_134597
591)del		GRCh38.p12First PassNC_000011.10Chr11134,483,002134,486,015134,596,762134,597,591
nssv14249888RemappedPerfectNC_000011.10:g.(13
4483002_134486015)
_(134602316_134605
788)del		GRCh38.p12First PassNC_000011.10Chr11134,483,002134,486,015134,602,316134,605,788
nssv14244950RemappedPerfectNC_000011.9:g.(134
352896_134355909)_
(134466656_1344674
85)del		GRCh37.p13First PassNC_000011.9Chr11134,352,896134,355,909134,466,656134,467,485
nssv14249888RemappedPerfectNC_000011.9:g.(134
352896_134355909)_
(134472210_1344756
82)del		GRCh37.p13First PassNC_000011.9Chr11134,352,896134,355,909134,472,210134,475,682
nssv14244950Submitted genomicNC_000011.8:g.(133
858106_133861119)_
(133971866_1339726
95)del		NCBI36 (hg18)NC_000011.8Chr11133,858,106133,861,119133,971,866133,972,695
nssv14249888Submitted genomicNC_000011.8:g.(133
858106_133861119)_
(133977420_1339808
92)del		NCBI36 (hg18)NC_000011.8Chr11133,858,106133,861,119133,977,420133,980,892

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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