A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690958



Internal ID15080924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4196512..4283616hg38UCSC Ensembl
Innerchr3:4238196..4325300hg19UCSC Ensembl
Innerchr3:4213196..4300300hg18UCSC Ensembl
Innerchr3:4213196..4300300hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3887105
hg1987105
hg1887105
hg1787105
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516589
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690958
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