A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653183



Internal ID15043149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133464689..133563944hg38UCSC Ensembl
Innerchr10:135278193..135377448hg19UCSC Ensembl
Innerchr10:135128183..135227438hg18UCSC Ensembl
Innerchr10:135167074..135266329hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3899256
hg1999256
hg1899256
hg1799256
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517180
Supporting Variants
Samples
Known GenesCYP2E1, SCART1, SYCE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653183
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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