A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258134



Internal ID21399366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84191211..84403668hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38212458
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730146
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258134
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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