A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082043



Internal ID21991276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51037683..51037683hg38UCSC Ensembl
chr17:49115044..49115044hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635968
Samples
Known GenesSPAG9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082043
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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