A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852873



Internal ID22627808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16465732..16474876hg38UCSC Ensembl
chr11:16487279..16496423hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg389145
hg199145
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457889
Samples
Known GenesSOX6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852873
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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