A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556776



Internal ID20929847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97367709..97368385hg38UCSC Ensembl
chr8:98379937..98380613hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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