A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519203



Internal ID15099810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28781383..28848861hg38UCSC Ensembl
Innerchr1:29107895..29175373hg19UCSC Ensembl
Innerchr1:28980482..29047960hg18UCSC Ensembl
Innerchr1:28928511..28995989hg17UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3867479
hg1967479
hg1867479
hg1767479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696691
Samples
Known GenesOPRD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519203
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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