A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548514



Internal ID20921700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64319101..64327300hg38UCSC Ensembl
chr20:62950454..62958653hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4508n223
Supporting Variantsnssv18203461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548514
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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