A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614166



Internal ID16054889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35662254..35705089hg38UCSC Ensembl
Innerchr9:35662251..35705086hg19UCSC Ensembl
Innerchr9:35652251..35695086hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3842836
hg1942836
hg1842836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176065
SamplesNINDS_65
Known GenesARHGEF39, CA9, TLN1, TPM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614166
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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