A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266664



Internal ID20475882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132680592..132680662hg38UCSC Ensembl
chr5:132016284..132016354hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747769
Supporting Variants
Samples
Known GenesIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266664
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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