A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559638



Internal ID332667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14877769..14878872hg38UCSC Ensembl
chr11:14899315..14900418hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041434
Samples
Known GenesCYP2R1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559638
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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