A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1052335



Internal ID15905521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31269628..31270746hg38UCSC Ensembl
Innerchr6:31237405..31238523hg19UCSC Ensembl
Innerchr6:31345384..31346502hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg381119
hg191119
hg181119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601505
Supporting Variants
Samples
Known GenesHLA-C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1052335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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