A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554488



Internal ID20927582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48876201..48893307hg38UCSC Ensembl
chr20:47492738..47509844hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3817107
hg1917107
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202968
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554488
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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