A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198753



Internal ID20765793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:105413101..105519000hg38UCSC Ensembl
chr1:105955723..106061622hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38105900
hg19105900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198753
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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