A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696245



Internal ID15432897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112679370..112785272hg38UCSC Ensembl
Innerchr13:113333684..113439586hg19UCSC Ensembl
Innerchr13:112381685..112487587hg18UCSC Ensembl
Innerchr13:112381685..112487587hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38105903
hg19105903
hg18105903
hg17105903
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518792
Supporting Variants
Samples
Known GenesATP11A, C13orf35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696245
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer