A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664400



Internal ID15054366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133563944hg38UCSC Ensembl
Innerchr10:135266389..135377448hg19UCSC Ensembl
Innerchr10:135116379..135227438hg18UCSC Ensembl
Innerchr10:135155270..135266329hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38111060
hg19111060
hg18111060
hg17111060
Variant TypeCNV gain
Copy Number
Allele State
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)nssv664400
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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