A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472282



Internal ID22530174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67618184..67620011hg38UCSC Ensembl
chr16:67652087..67653914hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381828
hg191828
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5870501
Supporting Variants
Samples
Known GenesCTCF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472282
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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