A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5514581



Internal ID291078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57273222..57306471hg38UCSC Ensembl
chr15:57565420..57598669hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3833250
hg1933250
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700831
Samples
Known GenesLINC00926, TCF12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5514581
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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