A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257059



Internal ID21399617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46486180..46489591hg38UCSC Ensembl
chr10:47059846..47063272hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg383412
hg193427
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730095
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257059
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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