A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475753



Internal ID22533651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62072964..62082094hg38UCSC Ensembl
chr17:60150325..60159455hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg389131
hg199131
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475753
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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