A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067082



Internal ID21976315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9353312..9353312hg38UCSC Ensembl
chr5:9353424..9353424hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542665
Samples
Known GenesSEMA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067082
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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