A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278395



Internal ID20845435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61611545..61623916hg38UCSC Ensembl
chr8:62524104..62536475hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3812372
hg1912372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566674
Supporting Variants
Samples
Known GenesASPH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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