A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584558



Internal ID21533100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30526427..30526742hg38UCSC Ensembl
chr19:31017334..31017649hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104570
SamplesNA19983
Known GenesZNF536
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584558
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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