A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486259



Internal ID21143812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50072062..50072686hg38UCSC Ensembl
chr13:50646198..50646822hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009469
Samples
Known GenesDLEU2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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