A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665437



Internal ID15402089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36107282..36137569hg38UCSC Ensembl
Innerchr17:34434675..34464949hg19UCSC Ensembl
Innerchr17:31458788..31489062hg18UCSC Ensembl
Innerchr17:31458788..31489062hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3830288
hg1930275
hg1830275
hg1730275
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517262
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665437
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