A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3591817



Internal ID18890098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6267015..6299812hg38UCSC Ensembl
Innerchr3:6308702..6341499hg19UCSC Ensembl
Innerchr3:6283702..6316499hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3832798
hg1932798
hg1832798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012973
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)nssv3591817
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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