A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705499



Internal ID21227300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:108900757..108900807hg38UCSC Ensembl
chr9:111663037..111663087hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819036
Supporting Variants
Samples
Known GenesIKBKAP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705499
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.177419


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