A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733762



Internal ID19032043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:76279831..76440879hg38UCSC Ensembl
Innerchr3:76328982..76490030hg19UCSC Ensembl
Innerchr3:76411672..76572720hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38161049
hg19161049
hg18161049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997619
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)nssv3733762
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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