A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756469



Internal ID20532329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997612..166997832hg38UCSC Ensembl
chr6:167411100..167411320hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285775
Samples
Known GenesMIR3939
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756469
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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