A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053870



Internal ID15907056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32019422..32023513hg38UCSC Ensembl
Innerchr6:31987199..31991290hg19UCSC Ensembl
Innerchr6:32095177..32099268hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384092
hg194092
hg184092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602088
Supporting Variants
Samples
Known GenesC4A, C4B, C4B_2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053870
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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