A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1954n223



Internal ID22804922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87799901..87840800hg38UCSC Ensembl
chr13:88452156..88493055hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3840900
hg1940900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6484505, nsv6477190
Samples
Known GenesLINC00397
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1954n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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