A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689058



Internal ID15425710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122083008..122086975hg38UCSC Ensembl
Innerchr10:123842523..123846490hg19UCSC Ensembl
Innerchr10:123832513..123836480hg18UCSC Ensembl
Innerchr10:123832513..123836480hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383968
hg193968
hg183968
hg173968
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519434
Supporting Variants
Samples
Known GenesTACC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689058
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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