A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851128



Internal ID22626063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15017436..15019235hg38UCSC Ensembl
chr11:15038982..15040781hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851128
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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