A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701928



Internal ID15438580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95523780..95534321hg38UCSC Ensembl
Innerchr13:96176034..96186575hg19UCSC Ensembl
Innerchr13:94974035..94984576hg18UCSC Ensembl
Innerchr13:94974035..94984576hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3810542
hg1910542
hg1810542
hg1710542
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525760
Supporting Variants
Samples
Known GenesCLDN10, CLDN10-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701928
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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