A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744236



Internal ID20520233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68415628..68415938hg38UCSC Ensembl
chr11:68183096..68183406hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267025
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744236
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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