A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493793



Internal ID22551723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120578690..120579789hg38UCSC Ensembl
chr5:119914385..119915484hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5841359
Supporting Variants
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493793
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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