A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3952n223



Internal ID22806920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85101375..85102141hg38UCSC Ensembl
chr2:85328498..85329264hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6553232, nsv6546413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3952n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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