A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv806n223



Internal ID22803774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73178211..73179308hg38UCSC Ensembl
chr10:74937969..74939066hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6575819, nsv6579693
Samples
Known GenesFAM149B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv806n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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