A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985023



Internal ID21894366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9063674..9063994hg38UCSC Ensembl
chr1:9123733..9124053hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529000
Samples
Known GenesSLC2A5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985023
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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