A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921386



Internal ID22696609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19618240..19618399hg38UCSC Ensembl
chr11:19639786..19639945hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361749
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921386
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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