A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3923n223



Internal ID22806891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70914185..70915080hg38UCSC Ensembl
chr2:71141315..71142210hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6553253, nsv6541455
Samples
Known GenesVAX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3923n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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