A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540924



Internal ID20914211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42009969..42026499hg38UCSC Ensembl
chr20:40638609..40655139hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3816531
hg1916531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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