A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111710



Internal ID20678750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159101801..159104300hg38UCSC Ensembl
chr4:160022953..160025452hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391902
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111710
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.04979


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