A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955104



Internal ID37377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119492105..119492168hg38UCSC Ensembl
chr4:120413260..120413323hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5468651
Supporting Variants
Samples
Known GenesLOC645513
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955104
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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