A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441488



Internal ID22107669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85906767..85907002hg38UCSC Ensembl
chr11:85617810..85618045hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756026
Samples
Known GenesCCDC83
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SUBSDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441488
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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