A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615562



Internal ID16402971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131394343..131394949hg38UCSC Ensembl
Innerchr9:134269730..134270336hg19UCSC Ensembl
Innerchr9:133259551..133260157hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38607
hg19607
hg18607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1145317
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615562
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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