A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496155



Internal ID273239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119034402..119037698hg38UCSC Ensembl
chr10:120793914..120797210hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383297
hg193297
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039302
Samples
Known GenesEIF3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496155
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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