A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039966



Internal ID18782497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69442388..69566648hg38UCSC Ensembl
Innerchr9:72057304..72181564hg19UCSC Ensembl
Innerchr9:71247124..71371384hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38124261
hg19124261
hg18124261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696246
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039966
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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