A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279002



Internal ID20846042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90016832..90018769hg38UCSC Ensembl
chr8:91029060..91030997hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573002
Supporting Variants
Samples
Known GenesDECR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279002
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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