A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596242



Internal ID18894523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:82662952..82719539hg38UCSC Ensembl
Innerchr3:82712103..82768690hg19UCSC Ensembl
Innerchr3:82794793..82851380hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3856588
hg1956588
hg1856588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008386
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3596242
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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