A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720845



Internal ID144511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5684673..5684688hg38UCSC Ensembl
chr19:5684684..5684699hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546886
Supporting Variants
Samples
Known GenesHSD11B1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720845
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002966


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