A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198737



Internal ID20765777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104726844..104739902hg38UCSC Ensembl
chr1:105269466..105282524hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3813059
hg1913059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332419
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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