A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958053



Internal ID16252009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5315847..5499313hg38UCSC Ensembl
Innerchr3:5357532..5541000hg19UCSC Ensembl
Innerchr3:5332532..5516000hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38183467
hg19183469
hg18183469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589458
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)nssv958053
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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