A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615561



Internal ID16402970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131394104..131394838hg38UCSC Ensembl
Innerchr9:134269491..134270225hg19UCSC Ensembl
Innerchr9:133259312..133260046hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38735
hg19735
hg18735
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12918n54
Supporting Variantsnssv1145315, nssv1145314, nssv1145316
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615561
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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