A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511932



Internal ID288500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49853813..49862745hg38UCSC Ensembl
chr14:50320531..50329463hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg388933
hg198933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511932
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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