A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208289



Internal ID20775329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201173375..201173838hg38UCSC Ensembl
chr2:202038098..202038561hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347739
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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