A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866448



Internal ID22641383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47144169..47151401hg38UCSC Ensembl
chr11:47165720..47172952hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg387233
hg197233
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467398
Samples
Known GenesC11orf49
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866448
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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