A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051846



Internal ID15558346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29888682..29929674hg38UCSC Ensembl
Innerchr6:29856459..29897451hg19UCSC Ensembl
Innerchr6:29964438..30005430hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3840993
hg1940993
hg1840993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601296
Supporting Variants
Samples
Known GenesHCG4B, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051846
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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