A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424361



Internal ID203354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32505924..32505975hg38UCSC Ensembl
chr12:32658858..32658909hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17055594
Samples
Known GenesFGD4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424361
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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