A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971318



Internal ID22746253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27698223..27698223hg38UCSC Ensembl
chr11:27719770..27719770hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351664
Samples
Known GenesBDNF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971318
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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