A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484213



Internal ID21141766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53380840..53381361hg38UCSC Ensembl
chr13:53954975..53955496hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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