A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971855



Internal ID48590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106816077..106867685hg38UCSC Ensembl
chr5:106151778..106203386hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3851609
hg1951609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463193
Supporting Variants
Samples
Known GenesLOC102467213
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971855
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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