A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696588



Internal ID15086554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:62727168..62727376hg38UCSC Ensembl
Innerchr3:62712843..62713051hg19UCSC Ensembl
Innerchr3:62687883..62688091hg18UCSC Ensembl
Innerchr3:62687883..62688091hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38209
hg19209
hg18209
hg17209
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517777
Supporting Variants
Samples
Known GenesCADPS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696588
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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