A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016472



Internal ID19105691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63542265..63763076hg38UCSC Ensembl
Innerchr9:67983175..68358810hg19UCSC Ensembl
Innerchr9:67572995..67848630hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38220812
hg19375636
hg18275636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3694817
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)nsv1016472
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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