A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892545



Internal ID169217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174233466..174234564hg38UCSC Ensembl
chr1:174202604..174203702hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418289
Supporting Variants
Samples
Known GenesRABGAP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892545
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.069332


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