A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472182



Internal ID22530074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6126403..6211337hg38UCSC Ensembl
chr16:6176404..6261338hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3884935
hg1984935
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868727
Supporting Variants
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472182
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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