A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561959



Internal ID21886314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161377273..161404564hg38UCSC Ensembl
chr5:160804279..160831570hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3827292
hg1927292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018203
Supporting Variants
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561959
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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