A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257420



Internal ID21399291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6031509..6364190hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38332682
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730046
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257420
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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