A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208303



Internal ID20775343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202341851..202358992hg38UCSC Ensembl
chr2:203206574..203223715hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3817142
hg1917142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352625
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208303
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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