A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489021



Internal ID21146574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107422876..107433917hg38UCSC Ensembl
chr13:108075224..108086265hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3811042
hg1911042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007167
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489021
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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