A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917180



Internal ID22692399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17349030..17355867hg38UCSC Ensembl
chr11:17370577..17377414hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386838
hg196838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361175
Samples
Known GenesNCR3LG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917180
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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