A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767166



Internal ID22101648
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 StatusS
Merged Variantsnsv4440662
Supporting Variants
Samples
Known GenesADRA1D
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767166
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer