A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257366



Internal ID21397978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95457928..95622782hg38UCSC Ensembl
chr2:96123676..96288530hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38164855
hg19164855
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730053
Supporting Variants
SamplesHG00512
Known GenesTRIM43, TRIM43B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257366
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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