A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257762



Internal ID21400206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:17863396..18357550hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38494155
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730259
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257762
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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