A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385307



Internal ID22443177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38278
hg19n/a
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975071
Supporting Variants
Samples
Known GenesPIGL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385307
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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