A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096359



Internal ID22005592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35552654..35552654hg38UCSC Ensembl
chr17:33879673..33879673hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621776
Samples
Known GenesSLFN14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096359
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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