A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278112



Internal ID20845152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47775129..47775906hg38UCSC Ensembl
chr8:48687690..48688467hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575180
Supporting Variants
Samples
Known GenesPRKDC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278112
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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