A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527354



Internal ID20900715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:12139001..12299000hg38UCSC Ensembl
chr20:12119649..12279648hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38160000
hg19160000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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