A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598963



Internal ID21547595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:48153754..48153819hg38UCSC Ensembl
chr19:48657011..48657076hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105106
SamplesHG03371
Known GenesLIG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598963
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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