A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4267n223



Internal ID22807235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206195955..206197001hg38UCSC Ensembl
chr2:207060679..207061725hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6539901, nsv6545319
Samples
Known GenesGPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4267n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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