A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519944



Internal ID20893305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4108199..4112167hg38UCSC Ensembl
chr20:4088846..4092814hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383969
hg193969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519944
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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