A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15707098



Internal ID21379374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45867962..45868090hg38UCSC Ensembl
chr3:45909454..45909582hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4390466
Supporting Variants
Samples
Known GenesLZTFL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15707098
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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