A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257587



Internal ID21399889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6029141..6369136hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38339996
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730046
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257587
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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