A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485580



Internal ID21143133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70921634..70947381hg38UCSC Ensembl
chr13:71495766..71521513hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3825748
hg1925748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485580
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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