A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145473



Internal ID344678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40428874..40438874hg38UCSC Ensembl
chr19:40934781..40944781hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3810001
hg1910001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145473
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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