A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695658



Internal ID15432310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41011504..41012940hg38UCSC Ensembl
Innerchr2:41238644..41240080hg19UCSC Ensembl
Innerchr2:41092148..41093584hg18UCSC Ensembl
Innerchr2:41150295..41151731hg17UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg381437
hg191437
hg181437
hg171437
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515841
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695658
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