A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5398445



Internal ID177841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72221487..72221538hg38UCSC Ensembl
chr11:71932531..71932582hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047112
Samples
Known GenesFOLR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5398445
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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