A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208225



Internal ID20775265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128074721..128088040hg38UCSC Ensembl
chr2:128832295..128845614hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3813320
hg1913320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353718
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208225
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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