A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363152



Internal ID22588821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40312820..40317323hg38UCSC Ensembl
chr11:40334370..40338873hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg384504
hg194504
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915446
Supporting Variants
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363152
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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