A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699360



Internal ID15436012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14575589..14581447hg38UCSC Ensembl
Innerchr5:14575698..14581556hg19UCSC Ensembl
Innerchr5:14628698..14634556hg18UCSC Ensembl
Innerchr5:14628698..14634556hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg385859
hg195859
hg185859
hg175859
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523575
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699360
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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