A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596205



Internal ID18894486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:76603763..76707496hg38UCSC Ensembl
Innerchr3:76652914..76756647hg19UCSC Ensembl
Innerchr3:76735604..76839337hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38103734
hg19103734
hg18103734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001612
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)nssv3596205
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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