A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855774



Internal ID22630709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65685329..65690872hg38UCSC Ensembl
chr11:65452800..65458343hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385544
hg195544
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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