A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903344



Internal ID22678511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138735311..138738051hg38UCSC Ensembl
chr6:139056448..139059188hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg382741
hg192741
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421455
Samples
Known GenesLOC100507462
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903344
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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