A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766917



Internal ID22101392
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 StatusS
Merged Variantsnsv4440985
Supporting Variants
Samples
Known GenesUSP47
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766917
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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