A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108706



Internal ID22017939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182160421..182161424hg38UCSC Ensembl
chr4:183081574..183082577hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg381004
hg191004
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554694
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108706
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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