A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523979



Internal ID15104586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:79405544..79546128hg38UCSC Ensembl
Innerchr13:79979679..80120263hg19UCSC Ensembl
Innerchr13:78877680..79018264hg18UCSC Ensembl
Innerchr13:78877680..79018264hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38140585
hg19140585
hg18140585
hg17140585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699834
Samples
Known GenesNDFIP2, NDFIP2-AS1, RBM26, RBM26-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523979
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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