A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4137n223



Internal ID22807105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:139840039..139843468hg38UCSC Ensembl
chr2:140597608..140601037hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg383430
hg193430
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6537402, nsv6548102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4137n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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