A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5401473



Internal ID180850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63720880..63720931hg38UCSC Ensembl
chr6:64430776..64430827hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735535
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5401473
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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