A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691207



Internal ID15427859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65207571..65225832hg38UCSC Ensembl
Innerchr3:65193246..65211507hg19UCSC Ensembl
Innerchr3:65168286..65186547hg18UCSC Ensembl
Innerchr3:65168286..65186547hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3818262
hg1918262
hg1818262
hg1718262
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516641
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691207
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer