A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461966



Internal ID22519851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10229401..10232818hg38UCSC Ensembl
chr11:10250948..10254365hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383418
hg193418
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864540
Supporting Variants
Samples
Known GenesSBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461966
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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