A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694097



Internal ID15084063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126493103..126496287hg38UCSC Ensembl
Innerchr3:126211946..126215130hg19UCSC Ensembl
Innerchr3:127694636..127697820hg18UCSC Ensembl
Innerchr3:127694644..127697828hg17UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg383185
hg193185
hg183185
hg173185
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521785
Supporting Variants
Samples
Known GenesUROC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694097
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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