A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068048



Internal ID20635088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36411135..36416154hg38UCSC Ensembl
chr20:35039538..35044557hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg385020
hg195020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526039
Supporting Variants
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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