A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176351



Internal ID15853279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:53610102..53640959hg38UCSC Ensembl
Innerchr13:54184237..54215094hg19UCSC Ensembl
Innerchr13:53082238..53113095hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3830858
hg1930858
hg1830858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561679
Supporting Variants
Samples1780854061_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176351
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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