A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192593



Internal ID20759633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72247685..72249735hg38UCSC Ensembl
chr10:74007443..74009493hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382051
hg192051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192593
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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