A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518710



Internal ID15446003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129811015..129811104hg38UCSC Ensembl
Innerchr7:129450855..129450944hg19UCSC Ensembl
Innerchr7:129238091..129238180hg18UCSC Ensembl
Innerchr7:129044806..129044895hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3890
hg1990
hg1890
hg1790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694265
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518710
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer