A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976380



Internal ID16270336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:147493190..147581487hg38UCSC Ensembl
Innerchr3:147210977..147299274hg19UCSC Ensembl
Innerchr3:148693667..148781964hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3888298
hg1988298
hg1888298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591969
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)nssv976380
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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