A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv671n223



Internal ID22803639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29384765..30674089hg38UCSC Ensembl
chr10:29673694..30963018hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381289325
hg191289325
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6584945, nsv6593310
Samples
Known GenesKIAA1462, LYZL2, MAP3K8, MIR604, MIR7162, MIR938, MTPAP, PTCHD3P1, SVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv671n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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