A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206892



Internal ID20773932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36683301..36693400hg38UCSC Ensembl
chr2:36910444..36920543hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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