A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440662



Internal ID22106840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4227652..4227704hg38UCSC Ensembl
chr20:4208299..4208351hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767166
Samples
Known GenesADRA1D
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440662
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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