A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529922



Internal ID305922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57350452..57488224hg38UCSC Ensembl
chr15:57642650..57780422hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38137773
hg19137773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700835
Samples
Known GenesCGNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529922
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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