A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518719



Internal ID20892080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25343046..25362924hg38UCSC Ensembl
chr20:25323682..25343560hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3819879
hg1919879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202557
Samples
Known GenesABHD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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