A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922996



Internal ID22698222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111814220..111814307hg38UCSC Ensembl
chr11:111684944..111685031hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361347
Samples
Known GenesALG9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922996
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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