A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856581



Internal ID22631516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6027261..6033643hg38UCSC Ensembl
chr11:6048491..6054873hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386383
hg196383
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465815
Samples
Known GenesOR56A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856581
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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