A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603068



Internal ID21551729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14244253..14245649hg38UCSC Ensembl
chr19:14355065..14356461hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381397
hg191397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103168
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603068
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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