A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036976



Internal ID19126195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376297..20421743hg38UCSC Ensembl
Innerchr15:20581550..20626996hg19UCSC Ensembl
Innerchr15:18841564..18887010hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3845447
hg1945447
hg1845447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2275n100
Supporting Variantsnssv3714565
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036976
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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