A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913053



Internal ID22688269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55268110..55880081hg38UCSC Ensembl
chr11:55035586..55647557hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38611972
hg19611972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364806
Samples
Known GenesOR4A15, OR4A16, OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2, TRIM48, TRIM51HP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913053
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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