A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699569



Internal ID15436221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:113462824..113496943hg38UCSC Ensembl
Innerchr8:114475053..114509172hg19UCSC Ensembl
Innerchr8:114544229..114578348hg18UCSC Ensembl
Innerchr8:114544229..114578348hg17UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3834120
hg1934120
hg1834120
hg1734120
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523752
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699569
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