A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522024



Internal ID15449317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:94186987..94220221hg38UCSC Ensembl
Innerchr8:95199215..95232449hg19UCSC Ensembl
Innerchr8:95268391..95301625hg18UCSC Ensembl
Innerchr8:95268391..95301625hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3833235
hg1933235
hg1833235
hg1733235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv465n21
Supporting Variantsnssv694793
Samples
Known GenesCDH17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522024
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