A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087055



Internal ID21996288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:84797660..84797660hg38UCSC Ensembl
chr9:87412575..87412575hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589456
Samples
Known GenesNTRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087055
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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