A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493319



Internal ID21150872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50168401..50189100hg38UCSC Ensembl
chr13:50742537..50763236hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3820700
hg1920700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189100
Samples
Known GenesST13P4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493319
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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