A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976853



Internal ID16270809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154634371..154726082hg38UCSC Ensembl
Innerchr3:154352160..154443871hg19UCSC Ensembl
Innerchr3:155834854..155926565hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3891712
hg1991712
hg1891712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592078
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)nssv976853
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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