A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698118



Internal ID15088084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133536297hg38UCSC Ensembl
Innerchr10:135266389..135349801hg19UCSC Ensembl
Innerchr10:135116379..135199791hg18UCSC Ensembl
Innerchr10:135155270..135238682hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3883413
hg1983413
hg1883413
hg1783413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517180
Supporting Variants
Samples
Known GenesCYP2E1, SCART1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698118
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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