A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3478n223



Internal ID22806446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21518526..23675522hg38UCSC Ensembl
chr19:21701328..23858324hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg382156997
hg192156997
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6597352, nsv6598100, nsv6599769
Samples
Known GenesLOC100132815, LOC100996349, LOC440518, LOC641367, ZNF100, ZNF208, ZNF257, ZNF429, ZNF43, ZNF492, ZNF675, ZNF676, ZNF724P, ZNF728, ZNF729, ZNF730, ZNF91, ZNF98, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3478n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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