A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704684



Internal ID21376960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87644457..87644507hg38UCSC Ensembl
chr9:90259372..90259422hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389053
Supporting Variants
Samples
Known GenesDAPK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704684
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0114943


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