A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694803



Internal ID15084769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:151811221..151829475hg38UCSC Ensembl
Innerchr1:151783697..151801951hg19UCSC Ensembl
Innerchr1:150050321..150068575hg18UCSC Ensembl
Innerchr1:148596770..148615024hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3818255
hg1918255
hg1818255
hg1718255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516369
Supporting Variants
Samples
Known GenesRORC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694803
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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