A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566962



Internal ID21759005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176397350..176397524hg38UCSC Ensembl
chr5:175824351..175824525hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012348
Supporting Variants
Samples
Known GenesCLTB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566962
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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