A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4345375



Internal ID19841539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5016392..5434558hg38UCSC Ensembl
chr11:5037622..5455788hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38418167
hg19418167
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15787483
Samples
Known GenesHBB, HBBP1, HBD, HBE1, HBG1, HBG2, OR51B2, OR51B4, OR51B5, OR51B6, OR51M1, OR51Q1, OR51V1, OR52A1, OR52A5, OR52E2, OR52J3
MethodSequencing
AnalysisSV calls were generated using multi-algorithm consensus pipeline involving raw evidence assessment, filtering, clustering, genotyping, alternative allele structure resolution, and gene annotation. These methods are described in detail in the gnomAD-SV preprint [Collins*, Brand*, et al., bioRxiv (2019)|https://www.biorxiv.org/content/10.1101/578674v1], and are largely based on methods developed in [Werling et al., Nat. Genet. (2018)|https://www.ncbi.nlm.nih.gov/pubmed/29700473].
Platform
Commentscomplex variant
ReferencegnomAD_Structural_Variants
Pubmed ID12345678
Accession Number(s)nsv4345375
Frequency
Sample Size10847
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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