A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059984



Internal ID20627024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28825082..28858297hg38UCSC Ensembl
chr1:29151594..29184809hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3833216
hg1933216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320474
Supporting Variants
Samples
Known GenesOPRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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