A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697105



Internal ID15087071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29089598..29090866hg38UCSC Ensembl
Innerchr15:29381801..29383069hg19UCSC Ensembl
Innerchr15:27169093..27170361hg18UCSC Ensembl
Innerchr15:27169093..27170361hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381269
hg191269
hg181269
hg171269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515798
Supporting Variants
Samples
Known GenesAPBA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697105
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