A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256995



Internal ID21397809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:28639573..29045066hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38405494
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730184
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256995
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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