A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270558



Internal ID20479776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54029459..54029536hg38UCSC Ensembl
chr8:54942019..54942096hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745873
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270558
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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