A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473736



Internal ID22531629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38934668..38937318hg38UCSC Ensembl
chr17:37090921..37093571hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382651
hg192651
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875913
Supporting Variants
Samples
Known GenesFBXO47
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473736
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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