A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543711



Internal ID20916957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53535418..53547873hg38UCSC Ensembl
chr20:52151957..52164412hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3812456
hg1912456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543711
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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