A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860042



Internal ID22634977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9361035..9363769hg38UCSC Ensembl
chr11:9382582..9385316hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382735
hg192735
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860042
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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