A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730120



Internal ID21400931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52859504..52859534hg38UCSC Ensembl
chr3:52893520..52893550hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3831
hg1931
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16256107
SamplesHG00513
Known GenesTMEM110, TMEM110-MUSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730120
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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