A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17123069



Internal ID21467054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109001815..109001815hg38UCSC Ensembl
chr5:108337516..108337516hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637049
Supporting Variants
SamplesHG03065
Known GenesFER
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17123069
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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