A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199931



Internal ID20766971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211688268..211690180hg38UCSC Ensembl
chr1:211861610..211863522hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381913
hg191913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199931
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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