A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614916



Internal ID16402325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94483540..94511377hg38UCSC Ensembl
Innerchr9:97245822..97273659hg19UCSC Ensembl
Innerchr9:96285643..96313480hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3827838
hg1927838
hg1827838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139706
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614916
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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