A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492270



Internal ID269487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10479698..10493105hg38UCSC Ensembl
chr10:10521661..10535068hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3813408
hg1913408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17683717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492270
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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