A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051837



Internal ID15558337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29888682..29912863hg38UCSC Ensembl
Innerchr6:29856459..29880640hg19UCSC Ensembl
Innerchr6:29964438..29988619hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3824182
hg1924182
hg1824182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601291
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)nssv1051837
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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