A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3916n223



Internal ID22806884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68277290..68278062hg38UCSC Ensembl
chr2:68504422..68505194hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6539472, nsv6542206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3916n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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