A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677632



Internal ID15414284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:46616792..46623975hg38UCSC Ensembl
Innerchr8:47528414..47535597hg19UCSC Ensembl
Innerchr8:47647579..47654762hg18UCSC Ensembl
Innerchr8:47647579..47654762hg17UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg387184
hg197184
hg187184
hg177184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677632
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