A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850595



Internal ID22625530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96335501..96353194hg38UCSC Ensembl
chr11:96068665..96086358hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3817694
hg1917694
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456249
Samples
Known GenesCCDC82, MAML2, MIR1260B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850595
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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