A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278253



Internal ID20845293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54478594..54479176hg38UCSC Ensembl
chr8:55391154..55391736hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574164
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278253
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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