A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516722



Internal ID15444015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162136930..162262487hg38UCSC Ensembl
Innerchr3:161854718..161980275hg19UCSC Ensembl
Innerchr3:163337412..163462969hg18UCSC Ensembl
Innerchr3:163337420..163462977hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38125558
hg19125558
hg18125558
hg17125558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688308, nssv670439, nssv684262, nssv676504, nssv693533, nssv674835, nssv671571
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516722
Frequency
Sample Size2026
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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