A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760653



Internal ID20536513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105070603..105070603hg38UCSC Ensembl
chr6:105518478..105518478hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293438
Samples
Known GenesLIN28B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760653
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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