A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568310



Internal ID20941381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31149295..31149666hg38UCSC Ensembl
chr8:31006811..31007182hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277738
Samples
Known GenesWRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568310
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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