A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555245



Internal ID20928336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56179004..56188848hg38UCSC Ensembl
chr20:54754060..54763904hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg389845
hg199845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555245
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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