A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042220



Internal ID19131439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20336715..20406244hg38UCSC Ensembl
Innerchr15:20541968..20611497hg19UCSC Ensembl
Innerchr15:18801982..18871511hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3869530
hg1969530
hg1869530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2241n100
Supporting Variantsnssv3536232
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042220
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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