A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256107



Internal ID21398263
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730120
Supporting Variants
SamplesHG00513
Known GenesTMEM110, TMEM110-MUSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256107
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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