A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567740



Internal ID20940811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102665418..102665649hg38UCSC Ensembl
chr8:103677646..103677877hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567740
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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