A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766688



Internal ID20542548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57322134..57322134hg38UCSC Ensembl
chr10:59081894..59081894hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766688
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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