A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968810



Internal ID46532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87954186..87954248hg38UCSC Ensembl
chr5:87250003..87250065hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465276
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968810
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003122


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