A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613078



Internal ID16400487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1836746..1945517hg38UCSC Ensembl
Innerchr9:1836746..1945517hg19UCSC Ensembl
Innerchr9:1826746..1935517hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38108772
hg19108772
hg18108772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156426
Samples1780862125_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613078
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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