A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038966



Internal ID20606006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21674454..21675009hg38UCSC Ensembl
chr18:19254415..19254970hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535301
Supporting Variants
Samples
Known GenesABHD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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