A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481621



Internal ID21139174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68857601..68858400hg38UCSC Ensembl
chr13:69431733..69432532hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18012164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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