A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522978



Internal ID299229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64692226..64701052hg38UCSC Ensembl
chr15:64984425..64993251hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg388827
hg198827
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704220
Samples
Known GenesOAZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522978
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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