A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475423



Internal ID22533319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13101331..13102830hg38UCSC Ensembl
chr17:13004648..13006147hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884919
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475423
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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