A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1356n223



Internal ID22804324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:4550677..4551382hg38UCSC Ensembl
chr12:4659843..4660548hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6585066, nsv6580412
Samples
Known GenesRAD51AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1356n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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