A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143509



Internal ID342710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52230106..52238106hg38UCSC Ensembl
chr13:52804241..52812241hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143509
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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