A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760840



Internal ID20536700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6090887..6090887hg38UCSC Ensembl
chr10:6132850..6132850hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275774
Samples
Known GenesRBM17
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760840
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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