A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203469



Internal ID20770509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26298727..26299945hg38UCSC Ensembl
chr1:26625218..26626436hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381219
hg191219
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319738
Supporting Variants
Samples
Known GenesUBXN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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