A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207146



Internal ID20774187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:87634601..87636600hg38UCSC Ensembl
chr2:87934120..87936119hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01381


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