A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534517



Internal ID20907878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36548743..36555707hg38UCSC Ensembl
chr20:35177146..35184110hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg386965
hg196965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068057
Samples
Known GenesMYL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534517
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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