A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17551356



Internal ID21875711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78767370..78771006hg38UCSC Ensembl
chr5:78063193..78066829hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg383637
hg193637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17551356
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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