A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280251



Internal ID20489469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3508770..3508825hg38UCSC Ensembl
chr5:3508884..3508939hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747343
Supporting Variants
Samples
Known GenesLINC01019
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280251
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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