A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446066



Internal ID22112245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10902540..10902540hg38UCSC Ensembl
chr2:11042666..11042666hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760795
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446066
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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