A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555866



Internal ID329015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76652961..76652976hg38UCSC Ensembl
chr11:76364005..76364020hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048564
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555866
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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