A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816722



Internal ID16110678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85873919..85977236hg38UCSC Ensembl
Innerchr13:86448054..86551371hg19UCSC Ensembl
Innerchr13:85346055..85449372hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38103318
hg19103318
hg18103318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562610
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)nssv816722
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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