A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494069



Internal ID271228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103261738..103270487hg38UCSC Ensembl
chr14:103728075..103736824hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg388750
hg198750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494069
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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