A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441279



Internal ID22107459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43888043..43888349hg38UCSC Ensembl
chr11:43909593..43909899hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763726
Samples
Known GenesALKBH3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441279
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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