A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559539



Internal ID332571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32095661..32140459hg38UCSC Ensembl
chr11:32117207..32162005hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3844799
hg1944799
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044644
Samples
Known GenesRCN1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559539
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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