A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586478



Internal ID21535032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11365895..11366652hg38UCSC Ensembl
chr19:11476571..11477328hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103050
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586478
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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