A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051801



Internal ID15558301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29886178..29889309hg38UCSC Ensembl
Innerchr6:29853955..29857086hg19UCSC Ensembl
Innerchr6:29961934..29965065hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg383132
hg193132
hg183132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601265
Supporting Variants
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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