A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444212



Internal ID22110392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56710717..56710717hg38UCSC Ensembl
chr20:55285773..55285773hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767746
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444212
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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