A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176116



Internal ID15508107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110222386..110541405hg38UCSC Ensembl
Innerchr9:112984666..113303685hg19UCSC Ensembl
Innerchr9:112024487..112343506hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38319020
hg19319020
hg18319020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615152
Supporting Variants
Samples1780862339_A
Known GenesSVEP1, TXN, TXNDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176116
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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