A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280837



Internal ID20490055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4827316..4827500hg38UCSC Ensembl
chr10:4869508..4869692hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731550
Supporting Variants
Samples
Known GenesAKR1E2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280837
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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