A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554748



Internal ID20927839
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 StatusM
Merged Variants
Supporting Variantsnssv18203403
Samples
Known GenesTAF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554748
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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