A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490588



Internal ID267842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61164716..61165024hg38UCSC Ensembl
chr10:62924474..62924782hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490588
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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