A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854613



Internal ID22629548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67335255..67338417hg38UCSC Ensembl
chr11:67102726..67105888hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383163
hg193163
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458713
Samples
Known GenesLOC100130987
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854613
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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