A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594329



Internal ID21542927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27759411..27762822hg38UCSC Ensembl
chr19:28250319..28253730hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg383412
hg193412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104530
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594329
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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