A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121258



Internal ID20688298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98258881..98540092hg38UCSC Ensembl
chr4:99180032..99461243hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38281212
hg19281212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391149
Supporting Variants
Samples
Known GenesRAP1GDS1, TSPAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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