A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199741



Internal ID20766781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115137890..115139290hg38UCSC Ensembl
chr1:115680511..115681911hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199741
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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