A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407398



Internal ID186732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17733562..17733613hg38UCSC Ensembl
chr7:17773186..17773237hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407398
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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