A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200509



Internal ID20767549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154915830..154917297hg38UCSC Ensembl
chr1:154888306..154889773hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381468
hg191468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200509
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00026


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