A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544671



Internal ID20917908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50772299..50842606hg38UCSC Ensembl
chr20:49388836..49459143hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3870308
hg1970308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205275
Samples
Known GenesBCAS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544671
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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