A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584774



Internal ID21533318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:4820133..4820456hg38UCSC Ensembl
chr17:4723428..4723751hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082229
SamplesNA19239
Known GenesPLD2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584774
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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