A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3915n223



Internal ID22806883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68154284..68155506hg38UCSC Ensembl
chr2:68381416..68382638hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381223
hg191223
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6543348, nsv6547539
Samples
Known GenesWDR92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3915n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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