A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068421



Internal ID20635461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47206294..47207605hg38UCSC Ensembl
chr20:45834938..45836249hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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