A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489917



Internal ID21147470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49972683..49990310hg38UCSC Ensembl
chr13:50546819..50564446hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3817628
hg1917628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009457
Samples
Known GenesDLEU2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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