A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200243



Internal ID20767283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54208427..54305909hg38UCSC Ensembl
chr19:54712295..54817192hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3897483
hg19104898
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528957
Supporting Variants
Samples
Known GenesLILRA3, LILRA6, LILRB2, LILRB3, LILRB5, MIR4752
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200243
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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