A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440985



Internal ID22107163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11854051..11855011hg38UCSC Ensembl
chr11:11875598..11876558hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766917
Samples
Known GenesUSP47
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440985
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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