A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704553



Internal ID21376829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138504640..138504983hg38UCSC Ensembl
chr8:139516883..139517226hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388935
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704553
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.16954


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