A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007616



Internal ID21916959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132680654..132680724hg38UCSC Ensembl
chr5:132016346..132016416hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551887
Samples
Known GenesIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007616
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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