A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187853



Internal ID20754893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71212101..71213700hg38UCSC Ensembl
chr10:72971858..72973457hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444014
Supporting Variants
Samples
Known GenesUNC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187853
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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