A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817536



Internal ID16111492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95258472..95265809hg38UCSC Ensembl
Innerchr13:95910726..95918063hg19UCSC Ensembl
Innerchr13:94708727..94716064hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg387338
hg197338
hg187338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562769
Supporting Variants
Samples
Known GenesABCC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817536
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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