A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861111



Internal ID22636046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19981982..19983781hg38UCSC Ensembl
chr11:20003528..20005327hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456582
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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