A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199592



Internal ID20766632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4860904..4900519hg38UCSC Ensembl
chr19:4860916..4900531hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3839616
hg1939616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516954
Supporting Variants
Samples
Known GenesARRDC5, PLIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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