A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655996



Internal ID18954277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32481746..32550980hg38UCSC Ensembl
Innerchr6:32449523..32518757hg19UCSC Ensembl
Innerchr6:32557501..32626735hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3869235
hg1969235
hg1869235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019273
Supporting Variants
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655996
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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