A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049390



Internal ID20616431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7834051..7837094hg38UCSC Ensembl
chr19:7898937..7901980hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383044
hg193044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531818
Supporting Variants
Samples
Known GenesEVI5L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049390
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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