A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420119



Internal ID22477989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109001815..109001815hg38UCSC Ensembl
chr5:108337516..108337516hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5960319
Supporting Variants
Samples
Known GenesFER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420119
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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