A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067497



Internal ID21976730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:59837780..59837780hg38UCSC Ensembl
chr5:59133606..59133606hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551189
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067497
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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