A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416516



Internal ID195737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91240401..91240452hg38UCSC Ensembl
chr15:91783631..91783682hg19UCSC Ensembl
Cytoband15q26.1
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 Variantsnssv17705143
Samples
Known GenesSV2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416516
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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