A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483363



Internal ID21140916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60181318..60227223hg38UCSC Ensembl
chr13:60755452..60801357hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3845906
hg1945906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18010559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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