A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890901



Internal ID168114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156522124..156525938hg38UCSC Ensembl
chr1:156491916..156495730hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg383815
hg193815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428039
Supporting Variants
Samples
Known GenesIQGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890901
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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