A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589477



Internal ID21781520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143942330..143942401hg38UCSC Ensembl
chr8:145016498..145016569hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010382
Supporting Variants
Samples
Known GenesPLEC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589477
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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