A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526488



Internal ID15453781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22932341..22959689hg38UCSC Ensembl
Innerchr2:23155213..23182561hg19UCSC Ensembl
Innerchr2:23008718..23036066hg18UCSC Ensembl
Innerchr2:23066865..23094213hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3827349
hg1927349
hg1827349
hg1727349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702797
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526488
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