A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286694



Internal ID20495912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146064590..146064676hg38UCSC Ensembl
chr5:145444153..145444239hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286694
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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