A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258663



Internal ID21399684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13060683..13168627hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38107945
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730073
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258663
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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