A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914654



Internal ID22689871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35367927..35367980hg38UCSC Ensembl
chr11:35389474..35389527hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355230
Samples
Known GenesSLC1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914654
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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