A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523919



Internal ID20897280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18261101..18266686hg38UCSC Ensembl
chr20:18241745..18247330hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg385586
hg195586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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