A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668357



Internal ID21616662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:472045..573542hg38UCSC Ensembl
chr19:472045..573542hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38101498
hg19101498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105447
Samples
Known GenesBSG, CDC34, GZMM, MADCAM1, ODF3L2, TPGS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668357
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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