A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035802



Internal ID19125021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240873..20793234hg38UCSC Ensembl
Innerchr15:20446126..20998563hg19UCSC Ensembl
Innerchr15:18706140..19258613hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38552362
hg19552438
hg18552474
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2209n100
Supporting Variantsnssv3534732, nssv3534731
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035802
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer