A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475055



Internal ID22532950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50298513..50321970hg38UCSC Ensembl
chr17:48375874..48399331hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3823458
hg1923458
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475055
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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