A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108913



Internal ID20675953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145976855..145981748hg38UCSC Ensembl
chr4:146898007..146902900hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg384894
hg194894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108913
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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