A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364178



Internal ID22589847
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 StatusS
Merged Variantsnsv5909729
Supporting Variants
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)nssv17364178
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.50


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