A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397266



Internal ID21054819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109564080..109571539hg38UCSC Ensembl
chr5:108899781..108907240hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg387460
hg197460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397266
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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