A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914762



Internal ID22689979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118413516..118414419hg38UCSC Ensembl
chr11:118284231..118285134hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38904
hg19904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353085
Samples
Known GenesLOC100131626
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914762
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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