A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531422



Internal ID307381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29534712..29534851hg38UCSC Ensembl
chr19:30025619..30025758hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722660
Samples
Known GenesVSTM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531422
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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