A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445661



Internal ID21103214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65390901..65397100hg38UCSC Ensembl
chr9:45733508..45739600hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg386200
hg196093
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7796n223
Supporting Variantsnssv18225445
Samples
Known GenesFAM27E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445661
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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