A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522109



Internal ID15449402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16868921..16906862hg38UCSC Ensembl
Innerchr7:16908545..16946486hg19UCSC Ensembl
Innerchr7:16875070..16913011hg18UCSC Ensembl
Innerchr7:16681785..16719726hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3837942
hg1937942
hg1837942
hg1737942
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694881
Samples
Known GenesAGR3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522109
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