A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509119



Internal ID285785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74494391..74494822hg38UCSC Ensembl
chr14:74961094..74961525hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699303
Samples
Known GenesISCA2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509119
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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