A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413917



Internal ID193206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60870925..60870976hg38UCSC Ensembl
chr15:61163124..61163175hg19UCSC Ensembl
Cytoband15q22.2
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 Variantsnssv17703184
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413917
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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