A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698905



Internal ID15435557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150420300..150422228hg38UCSC Ensembl
Innerchr6:150741436..150743364hg19UCSC Ensembl
Innerchr6:150783129..150785057hg18UCSC Ensembl
Innerchr6:150833550..150835478hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381929
hg191929
hg181929
hg171929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523189
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698905
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