A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294807



Internal ID20504025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34528518..34528642hg38UCSC Ensembl
chr8:34386036..34386160hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740206
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294807
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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