A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806778



Internal ID16100734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:25332787..25356520hg38UCSC Ensembl
Innerchr13:25906925..25930658hg19UCSC Ensembl
Innerchr13:24804925..24828658hg18UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3823734
hg1923734
hg1823734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561352
Supporting Variants
Samples
Known GenesNUPL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv806778
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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