A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540152



Internal ID20913444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39779101..39780900hg38UCSC Ensembl
chr20:38407743..38409542hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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