A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258096



Internal ID21399364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18180471..18357628hg38UCSC Ensembl
chrUn_gl000212:9223..186380hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38177158
hg19177158
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730259
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258096
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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