A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529287



Internal ID20902648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11377942..11388267hg38UCSC Ensembl
chr20:11358590..11368915hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3810326
hg1910326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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