A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256952



Internal ID21398915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5392710..6365792hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38973083
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730046
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256952
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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