A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496037



Internal ID273126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105462083..105462139hg38UCSC Ensembl
chr14:105928420..105928476hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700608
Samples
Known GenesMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496037
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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