A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865814



Internal ID22640749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60131677..60177829hg38UCSC Ensembl
chr11:59899150..59945302hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3846153
hg1946153
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464864, nssv17461711
Samples
Known GenesMS4A6A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865814
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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