A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492564



Internal ID269773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37874121..37876994hg38UCSC Ensembl
chr10:38163049..38165922hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg382874
hg192874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492564
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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