A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922129



Internal ID22697354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113055989..113077603hg38UCSC Ensembl
chr11:112926711..112948325hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3821615
hg1921615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362808
Samples
Known GenesNCAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922129
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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