A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735386



Internal ID20511328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96941352..96941727hg38UCSC Ensembl
chr10:98701109..98701484hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261367
Samples
Known GenesLCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735386
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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