A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758131



Internal ID20533991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76619299..76619299hg38UCSC Ensembl
chr11:76330343..76330343hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38497
hg19497
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758131
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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