A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569667



Internal ID20942738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98114357..98115398hg38UCSC Ensembl
chr8:99126585..99127626hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg381042
hg191042
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7431n223
Supporting Variantsnssv18279229
Samples
Known GenesHRSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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