A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289497



Internal ID20498715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174686162..174686375hg38UCSC Ensembl
chr5:174113165..174113378hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38214
hg19214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749279
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289497
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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