A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704445



Internal ID21376721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77469385..77469486hg38UCSC Ensembl
chr8:78381621..78381722hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388838
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704445
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.238506


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