A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014278



Internal ID21923621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80311318..80330464hg38UCSC Ensembl
chr5:79607137..79626283hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3819147
hg1919147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540986
Samples
Known GenesSPZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014278
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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