A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534396



Internal ID20907757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1489724..1503410hg38UCSC Ensembl
chr20:1470369..1484056hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3813687
hg1913688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066344
Samples
Known GenesSIRPB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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