A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866843



Internal ID22641778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73289380..73291522hg38UCSC Ensembl
chr11:73000425..73002567hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382143
hg192143
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458492
Samples
Known GenesP2RY6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866843
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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