A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909729



Internal ID22684939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55500571..56102471hg38UCSC Ensembl
chr11:55268047..55869947hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38601901
hg19601901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364178
Samples
Known GenesOR10AG1, OR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, OR5AS1, OR5D13, OR5D14, OR5D16, OR5D18, OR5F1, OR5I1, OR5L1, OR5L2, OR5W2, OR7E5P, OR8I2, TRIM51
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909729
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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