A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085516



Internal ID21994749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70029110..70029110hg38UCSC Ensembl
chr17:68025251..68025251hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085516
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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