A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704373



Internal ID21376649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29535358..29535774hg38UCSC Ensembl
chr8:29392875..29393291hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388773
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704373
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0143678


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