A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700219



Internal ID15436871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:90264186..90371181hg38UCSC Ensembl
Innerchr1:90729744..90836739hg19UCSC Ensembl
Innerchr1:90502332..90609327hg18UCSC Ensembl
Innerchr1:90441765..90548760hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38106996
hg19106996
hg18106996
hg17106996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524317
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700219
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