A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705637



Internal ID15442289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:27170182..27170770hg38UCSC Ensembl
Innerchr18:24750146..24750734hg19UCSC Ensembl
Innerchr18:23004144..23004732hg18UCSC Ensembl
Innerchr18:23004144..23004732hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38589
hg19589
hg18589
hg17589
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528945
Supporting Variants
Samples
Known GenesCHST9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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