A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444131



Internal ID22110311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62105808..62105808hg38UCSC Ensembl
chr20:60680864..60680864hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764117
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444131
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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