A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108225



Internal ID20675265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:117529912..117530315hg38UCSC Ensembl
chr4:118451067..118451470hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00127


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