A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441319



Internal ID22107499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58050631..58051631hg38UCSC Ensembl
chr11:57818103..57819103hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761628
Samples
Known GenesOR9Q1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441319
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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