A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958000



Internal ID15905270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3924671..4143342hg38UCSC Ensembl
Innerchr3:3966355..4185026hg19UCSC Ensembl
Innerchr3:3941355..4160026hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38218672
hg19218672
hg18218672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589403
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)nssv958000
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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