A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561908



Internal ID334875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:47021378..47021429hg38UCSC Ensembl
chr6:46989114..46989165hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984835
Samples
Known GenesGPR110
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561908
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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