A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730516



Internal ID20506428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9063679..9063998hg38UCSC Ensembl
chr1:9123738..9124057hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264733
Samples
Known GenesSLC2A5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730516
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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