A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv386n223



Internal ID22803354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153406708..153464211hg38UCSC Ensembl
chr1:153379184..153436687hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3857504
hg1957504
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6539573, nsv6550813
Samples
Known GenesS100A7, S100A7A, S100A7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv386n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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