A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437453



Internal ID21095006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67590301..67727100hg38UCSC Ensembl
chr9:44737462..46391453hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38136800
hg191653992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223147
Samples
Known GenesFAM27A, FAM27C, FAM27E1, FAM27E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437453
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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