A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487153



Internal ID21144706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109493331..109495016hg38UCSC Ensembl
chr13:110145678..110147363hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381686
hg191686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007950
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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