A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723569



Internal ID147235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45289343..45289726hg38UCSC Ensembl
chr19:45792601..45792984hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522991
Supporting Variants
Samples
Known GenesMARK4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723569
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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