A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257623



Internal ID21398275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30213188..30215917hg38UCSC Ensembl
chr20:29447864..29450593hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382730
hg192730
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730114
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257623
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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