A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546292



Internal ID20919510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54176070..54210925hg38UCSC Ensembl
chr20:52792609..52827464hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3834856
hg1934856
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203250
Samples
Known GenesPFDN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546292
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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