A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593428



Internal ID21785471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48775422..48776993hg38UCSC Ensembl
chr8:49687981..49689552hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381572
hg191572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593428
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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