A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539188



Internal ID20912492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56142242..56142711hg38UCSC Ensembl
chr20:54717298..54717767hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070397
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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