A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759492



Internal ID20535352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107654745..107654745hg38UCSC Ensembl
chr6:107975949..107975949hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296595
Samples
Known GenesSOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759492
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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