A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200514



Internal ID20767554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155105602..155117468hg38UCSC Ensembl
chr1:155078078..155089944hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3811867
hg1911867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200514
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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