A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053531



Internal ID15560031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31817661..31827305hg38UCSC Ensembl
Innerchr6:31785438..31795082hg19UCSC Ensembl
Innerchr6:31893417..31903061hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg389645
hg199645
hg189645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601949
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)nssv1053531
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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