A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178743



Internal ID20745783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47386441..47405745hg38UCSC Ensembl
chr10:48333617..48352921hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3819305
hg1919305
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439983
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178743
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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