A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443860



Internal ID22110041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35226721..35226721hg38UCSC Ensembl
chr20:33814524..33814524hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756508
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443860
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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