A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601291



Internal ID16042014
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 StatusM
Merged Variantsdgv10349n54
Supporting Variantsnssv1051837
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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