A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558612



Internal ID331671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87558581..87558626hg38UCSC Ensembl
chr11:87269473..87269518hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3846
hg1946
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558612
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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