A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281802



Internal ID20491020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84054867..84055452hg38UCSC Ensembl
chr5:83350686..83351271hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738066
Supporting Variants
Samples
Known GenesEDIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281802
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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