A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503739



Internal ID280555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51806371..51836541hg38UCSC Ensembl
chr13:52380507..52410677hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3830171
hg1930171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687765
Samples
Known GenesLINC00282
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503739
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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