A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15706448



Internal ID21378724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44691406..44691806hg38UCSC Ensembl
chr19:45194678..45195076hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38401
hg19399
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4392381
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15706448
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.158046


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