A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520886



Internal ID20894247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24835426..25188640hg38UCSC Ensembl
chr20:24816062..25169276hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38353215
hg19353215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202548
Samples
Known GenesACSS1, APMAP, CST7, LOC284798, VSX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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