A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540659



Internal ID294515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1471111..1471148hg38UCSC Ensembl
chr6:1471346..1471383hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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