A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521678



Internal ID15448971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34015906..34017533hg38UCSC Ensembl
Innerchr14:34485112..34486739hg19UCSC Ensembl
Innerchr14:33554863..33556490hg18UCSC Ensembl
Innerchr14:33554863..33556490hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381628
hg191628
hg181628
hg171628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698297
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521678
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