A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014515



Internal ID21923858
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 StatusM
Merged Variants
Supporting Variantsnssv17551356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014515
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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