A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695765



Internal ID15432417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18659832..18665366hg38UCSC Ensembl
Innerchr3:18701324..18706858hg19UCSC Ensembl
Innerchr3:18676328..18681862hg18UCSC Ensembl
Innerchr3:18676328..18681862hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg385535
hg195535
hg185535
hg175535
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518336
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695765
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