A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272659



Internal ID20481877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:92824101..92829666hg38UCSC Ensembl
chr5:92159808..92165373hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg385566
hg195566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733754
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272659
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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