A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517777



Internal ID15098384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62725627..62728634hg38UCSC Ensembl
Innerchr3:62711302..62714309hg19UCSC Ensembl
Innerchr3:62686342..62689349hg18UCSC Ensembl
Innerchr3:62686342..62689349hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg383008
hg193008
hg183008
hg173008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692332, nssv659755, nssv670168, nssv656406, nssv687616, nssv677925, nssv654481, nssv678197, nssv653213, nssv696588, nssv692614, nssv680487, nssv677875, nssv675265, nssv661022, nssv663131, nssv677536, nssv665364, nssv656981, nssv689402, nssv698604, nssv664317, nssv686453, nssv693384, nssv658129, nssv669514, nssv666521
Samples
Known GenesCADPS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517777
Frequency
Sample Size2026
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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