A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203403



Internal ID20770443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62047148..62054623hg38UCSC Ensembl
chr20:60622204..60629679hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387476
hg197476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554748
Supporting Variants
Samples
Known GenesTAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203403
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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