A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4390487



Internal ID21381622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57551966..57552331hg38UCSC Ensembl
chr3:57537693..57538058hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15707110
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4390487
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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