A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064999



Internal ID21974232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168718163..168718163hg38UCSC Ensembl
chr5:168145168..168145168hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566131
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064999
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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