A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584300



Internal ID21776343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124483026..124483113hg38UCSC Ensembl
chr8:125495267..125495354hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002102
Supporting Variants
Samples
Known GenesRNF139
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584300
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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