A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489133



Internal ID21146686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:55250441..55784894hg38UCSC Ensembl
chr13:55824576..56359028hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38534454
hg19534453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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