A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440959



Internal ID22107137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56365905..56366003hg38UCSC Ensembl
chr20:54940961..54941059hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766321
Samples
Known GenesFAM210B
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440959
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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