A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519314



Internal ID15446607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80383680..80399783hg38UCSC Ensembl
Innerchr10:82143436..82159539hg19UCSC Ensembl
Innerchr10:82133416..82149519hg18UCSC Ensembl
Innerchr10:82133416..82149519hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3816104
hg1916104
hg1816104
hg1716104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv47n21
Supporting Variantsnssv655353, nssv698116, nssv673702
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519314
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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