A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258681



Internal ID21399658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18212955..18355664hg38UCSC Ensembl
chrUn_gl000212:41707..184416hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38142710
hg19142710
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730259
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258681
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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