A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662446



Internal ID15052412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133556501hg38UCSC Ensembl
Innerchr10:135266389..135370005hg19UCSC Ensembl
Innerchr10:135116379..135219995hg18UCSC Ensembl
Innerchr10:135155270..135258886hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38103617
hg19103617
hg18103617
hg17103617
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)nssv662446
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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