A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922916



Internal ID22698141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133932279..133932495hg38UCSC Ensembl
chr11:133802174..133802390hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356500
Samples
Known GenesIGSF9B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922916
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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