A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851665



Internal ID22626600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27368535..27375334hg38UCSC Ensembl
chr11:27390082..27396881hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455593
Samples
Known GenesLGR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851665
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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