A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124222



Internal ID21477935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3509692..3509692hg38UCSC Ensembl
chr5:3509806..3509806hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638404
Supporting Variants
SamplesHG03486
Known GenesLINC01019
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124222
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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