A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv815784



Internal ID16109740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75962138..75989125hg38UCSC Ensembl
Innerchr13:76536274..76563261hg19UCSC Ensembl
Innerchr13:75434275..75461262hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3826988
hg1926988
hg1826988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562362
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)nssv815784
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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