A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199839



Internal ID20766879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192733041..192746212hg38UCSC Ensembl
chr1:192702171..192715342hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3813172
hg1913172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329552
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199839
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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