A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985399



Internal ID20552439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92205032..92205669hg38UCSC Ensembl
chr10:93964789..93965426hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446755
Supporting Variants
Samples
Known GenesCPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985399
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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