A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18117066



Internal ID20684106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39969582..39971194hg38UCSC Ensembl
chr4:39971202..39972814hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381613
hg191613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395404
Supporting Variants
Samples
Known GenesPDS5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18117066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00477


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