A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1054428



Internal ID15907614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32529033hg38UCSC Ensembl
Innerchr6:32455482..32496810hg19UCSC Ensembl
Innerchr6:32563460..32604788hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3841329
hg1941329
hg1841329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602162
Supporting Variants
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1054428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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