A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1649n223



Internal ID22804617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92066658..92067633hg38UCSC Ensembl
chr12:92460434..92461409hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6590920, nsv6579907
Samples
Known GenesC12orf79
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1649n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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