A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5396957



Internal ID176368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92964077..92964128hg38UCSC Ensembl
chr1:93429634..93429685hg19UCSC Ensembl
Cytoband1p22.1
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 Variantsnssv16906666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5396957
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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