A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103637



Internal ID20670677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67387773..67461789hg38UCSC Ensembl
chr3:67438197..67512213hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3874017
hg1974017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357527
Supporting Variants
Samples
Known GenesSUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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