A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526469



Internal ID20899830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17737675..17739269hg38UCSC Ensembl
chr20:17718320..17719914hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381595
hg191595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526469
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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