A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4261n223



Internal ID22807229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:203587387..203588718hg38UCSC Ensembl
chr2:204452110..204453441hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6539457, nsv6545962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4261n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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