A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590403



Internal ID21782446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41626348..41626455hg38UCSC Ensembl
chr8:41483867..41483974hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6018046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590403
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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