A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705076



Internal ID15095042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72911853..73049838hg38UCSC Ensembl
Innerchr10:74671611..74809596hg19UCSC Ensembl
Innerchr10:74341617..74479602hg18UCSC Ensembl
Innerchr10:74341617..74479602hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38137986
hg19137986
hg18137986
hg17137986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528473
Supporting Variants
Samples
Known GenesOIT3, P4HA1, PLA2G12B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705076
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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