A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530139



Internal ID306134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29520521..29520626hg38UCSC Ensembl
chr19:30011428..30011533hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722658
Samples
Known GenesLOC284395
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530139
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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