A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452922



Internal ID21110475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97411501..97412900hg38UCSC Ensembl
chr9:100173783..100175182hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234274
Samples
Known GenesTDRD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452922
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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