A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201611



Internal ID20768652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168731168..168751265hg38UCSC Ensembl
chr1:168700406..168720503hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3820098
hg1920098
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201611
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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