A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256426



Internal ID21399884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52261419..52289912hg38UCSC Ensembl
chr13:52835554..52864047hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3828494
hg1928494
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730069
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256426
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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