A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053538



Internal ID15560038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31817676..31826815hg38UCSC Ensembl
Innerchr6:31785453..31794592hg19UCSC Ensembl
Innerchr6:31893432..31902571hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg389140
hg199140
hg189140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601952
Supporting Variants
Samples
Known GenesHSPA1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053538
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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