A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519063



Internal ID20892424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20219846..20221685hg38UCSC Ensembl
chr20:20200490..20202329hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381840
hg191840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067031
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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