A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277936



Internal ID20844976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38519824..38521291hg38UCSC Ensembl
chr8:38377342..38378809hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg381468
hg191468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565589
Supporting Variants
Samples
Known GenesC8orf86
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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