A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257118



Internal ID21398262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144167049..144693513hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38526465
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730170
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257118
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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