A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200308



Internal ID20767348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102150801..102164400hg38UCSC Ensembl
chr1:102616357..102629956hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3813600
hg1913600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331965
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200308
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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