A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276412



Internal ID20843453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109310835..109312322hg38UCSC Ensembl
chr8:110323064..110324551hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381488
hg191488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571949
Supporting Variants
Samples
Known GenesNUDCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276412
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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