A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506790



Internal ID283525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101357088..101360167hg38UCSC Ensembl
chr14:101823425..101826504hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg383080
hg193080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506790
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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