A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890423



Internal ID167779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155017363..155017398hg38UCSC Ensembl
chr1:154989839..154989874hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552584
Supporting Variants
Samples
Known GenesZBTB7B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890423
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.133895


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