A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409510



Internal ID188831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35810568..35810619hg38UCSC Ensembl
chr1:36276169..36276220hg19UCSC Ensembl
Cytoband1p34.3
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 Variantsnssv16903703
Samples
Known GenesAGO4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409510
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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