A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208151



Internal ID20775191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213190482..213191424hg38UCSC Ensembl
chr2:214055206..214056148hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38943
hg19943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00123


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