A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505835



Internal ID282599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98474167..98575630hg38UCSC Ensembl
chr14:98940504..99041967hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38101464
hg19101464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17697293
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505835
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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