A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv970920



Internal ID16264876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102626794..103227372hg38UCSC Ensembl
Innerchr3:102345638..102946216hg19UCSC Ensembl
Innerchr3:103828328..104428906hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38600579
hg19600579
hg18600579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591190
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)nssv970920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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