A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701691



Internal ID15091657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28781383..28818676hg38UCSC Ensembl
Innerchr1:29107895..29145188hg19UCSC Ensembl
Innerchr1:28980482..29017775hg18UCSC Ensembl
Innerchr1:28928511..28965804hg17UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3837294
hg1937294
hg1837294
hg1737294
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525553
Supporting Variants
Samples
Known GenesOPRD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701691
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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