A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284489



Internal ID20493707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79717881..79718187hg38UCSC Ensembl
chr5:79013704..79014010hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746250
Supporting Variants
Samples
Known GenesCMYA5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284489
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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