A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446493



Internal ID22112672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38507980..38507980hg38UCSC Ensembl
chr21:39879904..39879904hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761760
Samples
Known GenesERG
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446493
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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