A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260024



Internal ID20469242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93766559..93766697hg38UCSC Ensembl
chr10:95526316..95526454hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734763
Supporting Variants
Samples
Known GenesLGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260024
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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