A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292191



Internal ID20501409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38077530..38080693hg38UCSC Ensembl
chr8:37935048..37938211hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg383164
hg193164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4748705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292191
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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