A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv52n199



Internal ID22802938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38769329..38793390hg38UCSC Ensembl
chr19:39259969..39284030hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3824062
hg1924062
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4756804, nsv4757491
Samples
Known GenesLGALS7, LGALS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv52n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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