A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15707110



Internal ID21379386
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 StatusS
Merged Variantsnsv4390487
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15707110
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.117816


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