A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1012865



Internal ID16306821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167822487..167874462hg38UCSC Ensembl
Innerchr4:168743638..168795613hg19UCSC Ensembl
Innerchr4:168980213..169032188hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3851976
hg1951976
hg1851976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596095
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1012865
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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