A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044488



Internal ID20611528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16461146..16464882hg38UCSC Ensembl
chr19:16571957..16575693hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383737
hg193737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529665
Supporting Variants
Samples
Known GenesEPS15L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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