A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209322



Internal ID20776362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48003782..48010752hg38UCSC Ensembl
chr3:48045272..48052242hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg386971
hg196971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361222
Supporting Variants
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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