A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525359



Internal ID20898720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7092760..7101523hg38UCSC Ensembl
chr20:7073407..7082170hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg388764
hg198764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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