A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419356



Internal ID22477226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168034067..168034122hg38UCSC Ensembl
chr5:167461072..167461127hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898070
Supporting Variants
Samples
Known GenesTENM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419356
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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