A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923606



Internal ID22698833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118499447..118499576hg38UCSC Ensembl
chr11:118370162..118370291hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351480
Samples
Known GenesKMT2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923606
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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