A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010273



Internal ID21919616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128070274..128076853hg38UCSC Ensembl
chr9:130832553..130839132hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386580
hg196580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592925
Samples
Known GenesSLC25A25
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010273
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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