A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525469



Internal ID20898830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19026296..19026965hg38UCSC Ensembl
chr20:19006940..19007609hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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