A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019994



Internal ID21929337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176962387..176962467hg38UCSC Ensembl
chr5:176389388..176389468hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561598
Samples
Known GenesUIMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019994
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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