A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4707n223



Internal ID22807675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40927639..40928285hg38UCSC Ensembl
chr22:41323643..41324289hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6598128, nsv6599710, nsv6598642
Samples
Known GenesXPNPEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4707n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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