A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407025



Internal ID186361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113202251..113202302hg38UCSC Ensembl
chr7:112842306..112842357hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407025
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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