A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493440



Internal ID21150993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109584589..109585223hg38UCSC Ensembl
chr13:110236936..110237570hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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