A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581936



Internal ID21773979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124470778..124493104hg38UCSC Ensembl
chr8:125483019..125505345hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3822327
hg1922327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014285
Supporting Variants
Samples
Known GenesRNF139, RNF139-AS1, TATDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581936
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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