A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105858



Internal ID20672898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120216745..120273807hg38UCSC Ensembl
chr4:121137900..121194962hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3857063
hg1957063
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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