A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668077



Internal ID15404729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44615589..44765525hg38UCSC Ensembl
Innerchr14:45084792..45234728hg19UCSC Ensembl
Innerchr14:44154542..44304478hg18UCSC Ensembl
Innerchr14:44154542..44304478hg17UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38149937
hg19149937
hg18149937
hg17149937
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517384
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668077
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