A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913454



Internal ID22688670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46659483..46665379hg38UCSC Ensembl
chr11:46681033..46686929hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg385897
hg195897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360608
Samples
Known GenesATG13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913454
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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