A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442516



Internal ID22108699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17778562..17778562hg38UCSC Ensembl
chr20:17759207..17759207hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766993
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442516
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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