A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723079



Internal ID146745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36239134..36239221hg38UCSC Ensembl
chr19:36730036..36730123hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723079
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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