A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053563



Internal ID15906749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31904199..31909078hg38UCSC Ensembl
Innerchr6:31871976..31876855hg19UCSC Ensembl
Innerchr6:31979955..31984834hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg384880
hg194880
hg184880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601969
Supporting Variants
Samples
Known GenesC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053563
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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