A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15756914



Internal ID22091390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10281081..10281081hg38UCSC Ensembl
chr2:10421207..10421207hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446043
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15756914
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer