A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278009



Internal ID20845049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41087910..41094525hg38UCSC Ensembl
chr8:40945429..40952044hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg386616
hg196616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278009
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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