A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699606



Internal ID15436258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18278938..18288347hg38UCSC Ensembl
Innerchr4:18280561..18289970hg19UCSC Ensembl
Innerchr4:17889659..17899068hg18UCSC Ensembl
Innerchr4:17956830..17966239hg17UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg389410
hg199410
hg189410
hg179410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523781
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699606
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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