A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860959



Internal ID22635894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115308088..115309271hg38UCSC Ensembl
chr11:115178808..115179991hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381184
hg191184
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465020
Samples
Known GenesCADM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860959
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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