A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656239



Internal ID15392891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29375578..29378586hg38UCSC Ensembl
Innerchr6:29343355..29346363hg19UCSC Ensembl
Innerchr6:29451334..29454342hg18UCSC Ensembl
Innerchr6:29451334..29454342hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg383009
hg193009
hg183009
hg173009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519453
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656239
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