A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476800



Internal ID21134353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:54096940..54097335hg38UCSC Ensembl
chr13:54671075..54671470hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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