A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474860



Internal ID22532755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11080906..11082016hg38UCSC Ensembl
chr17:10984223..10985333hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381111
hg191111
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5882931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474860
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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