A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053498



Internal ID15559998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31398818..31481199hg38UCSC Ensembl
Innerchr6:31366595..31448976hg19UCSC Ensembl
Innerchr6:31474574..31556955hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3882382
hg1982382
hg1882382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601921
Supporting Variants
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053498
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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