A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv979816



Internal ID15927086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001313..163003684hg38UCSC Ensembl
Innerchr3:162719101..162721472hg19UCSC Ensembl
Innerchr3:164201795..164204166hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382372
hg192372
hg182372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592371
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)nssv979816
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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