A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555025



Internal ID20928114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:51836759..51855684hg38UCSC Ensembl
chr20:50453298..50472223hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3818926
hg1918926
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555025
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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