A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404882



Internal ID184227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169065723..169065774hg38UCSC Ensembl
chr1:169034961..169035012hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891868
Samples
Known GenesLINC00970
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404882
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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