A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569395



Internal ID16010118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50053196..50145297hg38UCSC Ensembl
Innerchr15:50345393..50437494hg19UCSC Ensembl
Innerchr15:48132685..48224786hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3892102
hg1992102
hg1892102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842973
Samples
Known GenesATP8B4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569395
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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