A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145079



Internal ID20712119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5172459..5459724hg38UCSC Ensembl
chr6:5172693..5459957hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38287266
hg19287265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6395634
Supporting Variants
Samples
Known GenesFARS2, LYRM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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