A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051814



Internal ID15558314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29886431..29925418hg38UCSC Ensembl
Innerchr6:29854208..29893195hg19UCSC Ensembl
Innerchr6:29962187..30001174hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3838988
hg1938988
hg1838988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601273
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)nssv1051814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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