A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864433



Internal ID22639368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115729813..115735651hg38UCSC Ensembl
chr11:115600531..115606369hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385839
hg195839
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17466129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864433
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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