A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589778



Internal ID16030501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14765868..14823860hg38UCSC Ensembl
Innerchr3:14807375..14865367hg19UCSC Ensembl
Innerchr3:14782379..14840371hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3857993
hg1957993
hg1857993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959448
Samples
Known GenesC3orf20, FGD5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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