A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613668



Internal ID16401077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16310622..16377362hg38UCSC Ensembl
Innerchr9:16310620..16377360hg19UCSC Ensembl
Innerchr9:16300620..16367360hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3866741
hg1966741
hg1866741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1129286
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613668
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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