A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272477



Internal ID20481695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29382679..29382876hg38UCSC Ensembl
chr8:29240196..29240393hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739989
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272477
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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