A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048386



Internal ID20615426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4841355..4843229hg38UCSC Ensembl
chr19:4841367..4843241hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381875
hg191875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525701
Supporting Variants
Samples
Known GenesPLIN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048386
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00069


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