A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535022



Internal ID20908383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3435385..3440408hg38UCSC Ensembl
chr20:3416032..3421055hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385024
hg195024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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