A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100099



Internal ID21276897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:24673523..24727102hg38UCSC Ensembl
Innerchr18:22253487..22307066hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3853580
hg1953580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110319
Supporting Variants
Samplessample243
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100099
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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