A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4256n223



Internal ID22807224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202309122..202310639hg38UCSC Ensembl
chr2:203173845..203175362hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381518
hg191518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6541667, nsv6552772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4256n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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