A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14098754



Internal ID21269511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40933267..40962288hg38UCSC Ensembl
Innerchr18:38513231..38542252hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3829022
hg1929022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110244
Supporting Variants
Samplessample14
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14098754
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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