A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526342



Internal ID302475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64469627..64480488hg38UCSC Ensembl
chr15:64761826..64772687hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3810862
hg1910862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704199
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526342
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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