A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917202



Internal ID22692421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105610030..105611115hg38UCSC Ensembl
chr9:108372311..108373396hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441659
Samples
Known GenesFKTN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917202
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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