A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198743



Internal ID20765783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105006131..105016478hg38UCSC Ensembl
chr1:105548753..105559100hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3810348
hg1910348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198743
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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