A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1592n223



Internal ID22804560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70658905..70660045hg38UCSC Ensembl
chr12:71052685..71053825hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6587710, nsv6575808, nsv6592264
Samples
Known GenesPTPRR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1592n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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