A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055727



Internal ID15908913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32553420..32557458hg38UCSC Ensembl
Innerchr6:32521197..32525235hg19UCSC Ensembl
Innerchr6:32629175..32633213hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384039
hg194039
hg184039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602515
Supporting Variants
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055727
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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