A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668400



Internal ID21616705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37191088..37309822hg38UCSC Ensembl
chr19:37681990..37800724hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38118735
hg19118735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105161
Samples
Known GenesLOC284412, ZNF383, ZNF585B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668400
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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