A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057644



Internal ID15564144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33207006..33286888hg38UCSC Ensembl
Innerchr6:33174783..33254665hg19UCSC Ensembl
Innerchr6:33282761..33362643hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3879883
hg1979883
hg1879883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602831
Supporting Variants
Samples
Known GenesB3GALT4, HCG25, MIR219-1, RING1, RPS18, VPS52, WDR46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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