A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5544791



Internal ID318898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126361719..126361756hg38UCSC Ensembl
chr6:126682865..126682902hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969662
Samples
Known GenesCENPW
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5544791
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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