A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049396



Internal ID20616437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7887275..7889847hg38UCSC Ensembl
chr19:7952160..7954732hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382573
hg192573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519313
Supporting Variants
Samples
Known GenesLRRC8E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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