A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614746



Internal ID16402155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78357852..78432975hg38UCSC Ensembl
Innerchr9:80972768..81047891hg19UCSC Ensembl
Innerchr9:80162588..80237711hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3875124
hg1975124
hg1875124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176455
Samples1780862197_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614746
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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