A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484804



Internal ID21142357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68669501..68693700hg38UCSC Ensembl
chr13:69243633..69267832hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3824200
hg1924200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1901n223
Supporting Variantsnssv18012378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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