A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264733



Internal ID20473951
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 StatusS
Merged Variantsnsv4730516
Supporting Variants
Samples
Known GenesSLC2A5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264733
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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