A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189832



Internal ID20756872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47644101..47698800hg38UCSC Ensembl
chr10:49043087..49095536hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3854700
hg1952450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.07634


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