A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598528



Internal ID21547155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57017501..57017662hg38UCSC Ensembl
chr19:57528869..57529030hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106610
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598528
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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