A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087304



Internal ID21996537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57205493..57205493hg38UCSC Ensembl
chr17:55282854..55282854hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087304
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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