A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100063



Internal ID21275560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67754366..68189429hg38UCSC Ensembl
Innerchr18:65421603..65856666hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38435064
hg19435064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110737
Supporting Variants
Samplessample224
Known GenesLOC643542
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100063
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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