A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545181



Internal ID20918413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:60944663..61060715hg38UCSC Ensembl
chr20:59519719..59635771hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38116053
hg19116053
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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