A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560598



Internal ID21884953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173935551..173935615hg38UCSC Ensembl
chr5:173362554..173362618hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002509
Supporting Variants
Samples
Known GenesCPEB4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560598
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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