A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198813



Internal ID20765853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41468543..41524890hg38UCSC Ensembl
chr19:41974448..42031250hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3856348
hg1956803
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526395
Supporting Variants
Samples
Known GenesLOC100505495
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198813
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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