A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867330



Internal ID22642265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27454096..27464758hg38UCSC Ensembl
chr11:27475643..27486305hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3810663
hg1910663
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463124
Samples
Known GenesLGR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867330
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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