A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051765



Internal ID15558265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29927451hg38UCSC Ensembl
Innerchr6:29851443..29895228hg19UCSC Ensembl
Innerchr6:29959422..30003207hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3843786
hg1943786
hg1843786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601253
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)nssv1051765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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