A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443857



Internal ID22110038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33147364..33147364hg38UCSC Ensembl
chr20:31735170..31735170hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761882
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443857
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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