A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968682



Internal ID22743617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83714212..83714212hg38UCSC Ensembl
chr11:83425255..83425255hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363760
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968682
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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