A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18133433



Internal ID20700473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79626885..79629887hg38UCSC Ensembl
chr5:78922708..78925710hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg383003
hg193003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410327
Supporting Variants
Samples
Known GenesPAPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18133433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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