A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699108



Internal ID15089074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:60402952..60550127hg38UCSC Ensembl
Innerchr13:60977086..61124261hg19UCSC Ensembl
Innerchr13:59875087..60022262hg18UCSC Ensembl
Innerchr13:59875087..60022262hg17UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38147176
hg19147176
hg18147176
hg17147176
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523359
Supporting Variants
Samples
Known GenesTDRD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699108
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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