A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723565



Internal ID147231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45229224..45229313hg38UCSC Ensembl
chr19:45732482..45732571hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527525
Supporting Variants
Samples
Known GenesEXOC3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723565
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.089447


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