A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4187n223



Internal ID22807155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170900988..170901551hg38UCSC Ensembl
chr2:171757498..171758061hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6553733, nsv6539558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4187n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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