A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256468



Internal ID21398096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95430875..95649582hg38UCSC Ensembl
chr2:96096623..96315330hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38218708
hg19218708
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)nssv16256468
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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