A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490212



Internal ID21147765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:53273534..53276238hg38UCSC Ensembl
chr13:53847669..53850373hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg382705
hg192705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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