A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16899099



Internal ID170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19255719..19255865hg38UCSC Ensembl
chr1:19582213..19582359hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428180
Supporting Variants
Samples
Known GenesMRTO4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16899099
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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