A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856499



Internal ID22631434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70390846..70391945hg38UCSC Ensembl
chr11:70236952..70238051hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467833
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856499
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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