A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725676



Internal ID149342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55425925..55427768hg38UCSC Ensembl
chr19:55937292..55939135hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381844
hg191844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725676
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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