A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180103



Internal ID20747143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1939413..1950861hg38UCSC Ensembl
chr16:1989414..2000862hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3811449
hg1911449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500554
Supporting Variants
Samples
Known GenesMSRB1, RPL3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180103
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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