A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817662



Internal ID16111618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97867255..97888965hg38UCSC Ensembl
Innerchr13:98519509..98541219hg19UCSC Ensembl
Innerchr13:97317510..97339220hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3821711
hg1921711
hg1821711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562824
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)nssv817662
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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