A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924412



Internal ID22699639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96039906..96040714hg38UCSC Ensembl
chr11:95773070..95773878hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364927
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924412
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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