A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861173



Internal ID22636108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20096022..20104259hg38UCSC Ensembl
chr11:20117568..20125805hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg388238
hg198238
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455886
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861173
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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