A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560663



Internal ID333666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14393654..14393742hg38UCSC Ensembl
chr11:14415200..14415288hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560663
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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