A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580569



Internal ID21772612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72428972..72430793hg38UCSC Ensembl
chr8:73341207..73343028hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg381822
hg191822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001602
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580569
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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