A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698917



Internal ID15088883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15542583..16002971hg38UCSC Ensembl
Innerchr7:15582208..16042596hg19UCSC Ensembl
Innerchr7:15548733..16009121hg18UCSC Ensembl
Innerchr7:15355448..15815836hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38460389
hg19460389
hg18460389
hg17460389
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523199
Supporting Variants
Samples
Known GenesAGMO, MEOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698917
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