A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126054



Internal ID20693094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146550352..146559696hg38UCSC Ensembl
chr5:145929915..145939259hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg389345
hg199345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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