A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723338



Internal ID147004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39443231..39443715hg38UCSC Ensembl
chr19:39933871..39934355hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514132
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723338
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004061


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