A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403807



Internal ID183166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:109960761..109960812hg38UCSC Ensembl
chr10:111720519..111720570hg19UCSC Ensembl
Cytoband10q25.1
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 Variantsnssv17041031
Samples
Known GenesADD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403807
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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