A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615276



Internal ID16402685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123346788..123349072hg38UCSC Ensembl
Innerchr9:126109067..126111351hg19UCSC Ensembl
Innerchr9:125148888..125151172hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382285
hg192285
hg182285
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141303
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615276
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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