A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909582



Internal ID22684792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47203442..47203663hg38UCSC Ensembl
chr11:47224993..47225214hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909582
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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