A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723741



Internal ID147407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:47124769..47127007hg38UCSC Ensembl
chr19:47628026..47630264hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382239
hg192239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723741
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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