A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16966770



Internal ID45167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73581531..73590130hg38UCSC Ensembl
chr5:72877356..72885955hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462771
Supporting Variants
Samples
Known GenesUTP15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16966770
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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