A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561299



Internal ID21885654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30782264..30782345hg38UCSC Ensembl
chr8:30639780..30639861hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006141
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561299
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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