A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200250



Internal ID20767290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54221201..54237000hg38UCSC Ensembl
chr19:54725073..54740876hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815800
hg1915804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526515
Supporting Variants
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200250
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.2453


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