A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516375



Internal ID15443668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132043266..132054428hg38UCSC Ensembl
Innerchr3:131762110..131773272hg19UCSC Ensembl
Innerchr3:133244800..133255962hg18UCSC Ensembl
Innerchr3:133244808..133255970hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3811163
hg1911163
hg1811163
hg1711163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681166, nssv676265, nssv667847
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516375
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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