A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267170



Internal ID20476388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77973144..77973366hg38UCSC Ensembl
chr8:78885379..78885601hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736927
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267170
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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