A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7432n223



Internal ID22810400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98218783..98219693hg38UCSC Ensembl
chr8:99231011..99231921hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38911
hg19911
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6555682, nsv6571959
Samples
Known GenesNIPAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7432n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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