A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116055



Internal ID20683095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3895855..4169421hg38UCSC Ensembl
chr4:3897582..4171148hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38273567
hg19273567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368894
Supporting Variants
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00046


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