A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475468



Internal ID22533364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15606690..15629486hg38UCSC Ensembl
chr17:15510004..15532800hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3822797
hg1922797
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5880163
Supporting Variants
Samples
Known GenesCDRT1, TRIM16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475468
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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