A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505769



Internal ID282535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36755660..36757392hg38UCSC Ensembl
chr14:37224865..37226597hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg381733
hg191733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696904
Samples
Known GenesSLC25A21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505769
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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