A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277668



Internal ID20844708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30121554..30121997hg38UCSC Ensembl
chr8:29979070..29979513hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557809
Supporting Variants
Samples
Known GenesLEPROTL1, MIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277668
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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