A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17441659



Internal ID22499529
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 StatusS
Merged Variantsnsv5917202
Supporting Variants
Samples
Known GenesFKTN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17441659
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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