A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817396



Internal ID16111352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90600006..90652857hg38UCSC Ensembl
Innerchr13:91252260..91305111hg19UCSC Ensembl
Innerchr13:90050261..90103112hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3852852
hg1952852
hg1852852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562684
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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