A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518765



Internal ID20892126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3261546..3268990hg38UCSC Ensembl
chr20:3242192..3249636hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387445
hg197445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067398
Samples
Known GenesC20orf194
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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