A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681372



Internal ID15071338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:29255106..29272431hg38UCSC Ensembl
Innerchr15:29547310..29564635hg19UCSC Ensembl
Innerchr15:27334602..27351927hg18UCSC Ensembl
Innerchr15:27334602..27351927hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3817326
hg1917326
hg1817326
hg1717326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515660
Supporting Variants
Samples
Known GenesFAM189A1, NDNL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681372
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