A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977031



Internal ID22751966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115206758..115206758hg38UCSC Ensembl
chr11:115077478..115077478hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361096
Samples
Known GenesCADM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977031
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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