A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100626



Internal ID22009859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9957990..9975630hg38UCSC Ensembl
chr20:9938638..9956278hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3817641
hg1917641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100626
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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