A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525790



Internal ID15453083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:112722037..112723970hg38UCSC Ensembl
Innerchr2:113479614..113481547hg19UCSC Ensembl
Innerchr2:113196085..113198018hg18UCSC Ensembl
Innerchr2:113195845..113197778hg17UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg381934
hg191934
hg181934
hg171934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701970
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525790
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