A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851111



Internal ID22626046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74698103..74701809hg38UCSC Ensembl
chr11:74409148..74412854hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383707
hg193707
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462253
Samples
Known GenesCHRDL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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