A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691290



Internal ID15081256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133556028hg38UCSC Ensembl
Innerchr10:135266389..135369532hg19UCSC Ensembl
Innerchr10:135116379..135219522hg18UCSC Ensembl
Innerchr10:135155270..135258413hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38103144
hg19103144
hg18103144
hg17103144
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)nssv691290
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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