A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729395



Internal ID153061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44262287..44271636hg38UCSC Ensembl
chr22:44658167..44667516hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg389350
hg199350
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556078
Supporting Variants
Samples
Known GenesKIAA1644
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729395
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.002029


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