A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556232



Internal ID20929303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22339274..22340123hg38UCSC Ensembl
chr8:22196787..22197636hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277469
Samples
Known GenesPIWIL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556232
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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