A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516032



Internal ID292501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41358804..41359168hg38UCSC Ensembl
chr19:41864709..41865073hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723492
Samples
Known GenesB9D2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516032
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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