A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909391



Internal ID22684601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12934455..12934818hg38UCSC Ensembl
chr11:12956002..12956365hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356824
Samples
Known GenesTEAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909391
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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