A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722657



Internal ID146323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29514634..29514701hg38UCSC Ensembl
chr19:30005541..30005608hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5519532
Supporting Variants
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722657
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002344


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