A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516983



Internal ID15444276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13064011..13084531hg38UCSC Ensembl
Innerchr7:13103636..13124156hg19UCSC Ensembl
Innerchr7:13070161..13090681hg18UCSC Ensembl
Innerchr7:12876876..12897396hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3820521
hg1920521
hg1820521
hg1720521
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652788, nssv683313, nssv678739, nssv653552, nssv670261, nssv689947, nssv682685, nssv658134, nssv681349, nssv681091, nssv687537, nssv661751, nssv665882, nssv662827, nssv670380, nssv691491, nssv681178, nssv678023, nssv677110, nssv684582, nssv688179, nssv665977, nssv663506, nssv677757, nssv685388, nssv658698, nssv657327, nssv682814, nssv672273, nssv670493, nssv680524, nssv655573, nssv685887, nssv692180
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516983
Frequency
Sample Size2026
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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