A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540363



Internal ID20913654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54028101..54041500hg38UCSC Ensembl
chr20:52644640..52658039hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4494n223
Supporting Variantsnssv18067897
Samples
Known GenesBCAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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