A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955465



Internal ID37626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106525539..106545737hg38UCSC Ensembl
chr4:107446696..107466894hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3820199
hg1920199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955465
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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