A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971008



Internal ID22745943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32522015..32522015hg38UCSC Ensembl
chr11:32543561..32543561hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971008
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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