A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043379



Internal ID20610419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62759894..62763918hg38UCSC Ensembl
chr18:60427127..60431151hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg384025
hg194025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516536
Supporting Variants
Samples
Known GenesPHLPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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