A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444212



Internal ID21101765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105581863..105594368hg38UCSC Ensembl
chr9:108344144..108356649hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3812506
hg1912506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172364
Samples
Known GenesFKTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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