A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967766



Internal ID16261722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90269478..90340597hg38UCSC Ensembl
Innerchr3:90318628..90389747hg19UCSC Ensembl
Innerchr3:90401318..90472437hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3871120
hg1971120
hg1871120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590981
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)nssv967766
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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