A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074052



Internal ID21983285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68263097..68263097hg38UCSC Ensembl
chr5:67558925..67558925hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553891
Samples
Known GenesPIK3R1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074052
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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