A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278667



Internal ID20845707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73692496..73693171hg38UCSC Ensembl
chr8:74604731..74605406hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561044
Supporting Variants
Samples
Known GenesSTAU2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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