A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998197



Internal ID18844020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:79739743..79740145hg38UCSC Ensembl
Outerchr18:77499743..77500145hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146834
Supporting Variants
SamplesKWB1
Known GenesCTDP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998197
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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