A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614163



Internal ID16401572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35526073..35557737hg38UCSC Ensembl
Innerchr9:35526070..35557734hg19UCSC Ensembl
Innerchr9:35516070..35547734hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3831665
hg1931665
hg1831665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1132856
Samples
Known GenesRUSC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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