A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277548



Internal ID20844588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25355485..25355982hg38UCSC Ensembl
chr8:25213001..25213498hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564828
Supporting Variants
Samples
Known GenesDOCK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277548
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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