A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556807



Internal ID20929878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137979379..137980306hg38UCSC Ensembl
chr8:138991622..138992549hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277220
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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