A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516057



Internal ID15443350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8760797..8769210hg38UCSC Ensembl
Innerchr3:8802483..8810896hg19UCSC Ensembl
Innerchr3:8777483..8785896hg18UCSC Ensembl
Innerchr3:8777483..8785896hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388414
hg198414
hg188414
hg178414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665906, nssv659279, nssv673717, nssv692217, nssv661520, nssv660134, nssv687413, nssv676755, nssv673315
Samples
Known GenesOXTR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516057
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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