A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449719



Internal ID21107272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93009224..93012115hg38UCSC Ensembl
chr9:95771506..95774397hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382892
hg192892
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220653
Samples
Known GenesFGD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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