A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182669



Internal ID20749709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101245494..101255793hg38UCSC Ensembl
chr10:103005251..103015550hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182669
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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