A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516418



Internal ID15097025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100605598..100714748hg38UCSC Ensembl
Innerchr3:100324442..100433592hg19UCSC Ensembl
Innerchr3:101807132..101916282hg18UCSC Ensembl
Innerchr3:101807132..101916282hg17UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38109151
hg19109151
hg18109151
hg17109151
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669689, nssv664394, nssv684459, nssv671430, nssv660996, nssv659901, nssv662328, nssv692551, nssv678676, nssv687348, nssv691678, nssv678633, nssv656493, nssv652898, nssv671129, nssv673191, nssv662687, nssv659504, nssv658152, nssv661473, nssv660356
Samples
Known GenesGPR128, TFG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516418
Frequency
Sample Size2026
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


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