A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699752



Internal ID15436404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59897033..59899607hg38UCSC Ensembl
Innerchr18:57564265..57566839hg19UCSC Ensembl
Innerchr18:55715245..55717819hg18UCSC Ensembl
Innerchr18:55715245..55717819hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg382575
hg192575
hg182575
hg172575
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523909
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699752
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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