A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975618



Internal ID22750553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18209132..18209132hg38UCSC Ensembl
chr11:18230679..18230679hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357286
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975618
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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