A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405639



Internal ID184982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15768620..15768671hg38UCSC Ensembl
chr2:15908744..15908795hg19UCSC Ensembl
Cytoband2p24.3
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 Variantsnssv16909860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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