A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523200



Internal ID15103807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24446177..24505826hg38UCSC Ensembl
Innerchr14:24915383..24975032hg19UCSC Ensembl
Innerchr14:23985223..24044872hg18UCSC Ensembl
Innerchr14:23985223..24044872hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3859650
hg1959650
hg1859650
hg1759650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128n21
Supporting Variantsnssv698918
Samples
Known GenesCMA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523200
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer