A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1054453



Internal ID15907639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32554748hg38UCSC Ensembl
Innerchr6:32455482..32522525hg19UCSC Ensembl
Innerchr6:32563460..32630503hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3867044
hg1967044
hg1867044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602171
Supporting Variants
Samples
Known GenesHLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1054453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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