A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442814



Internal ID22108996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:868473..868473hg38UCSC Ensembl
chr7:908110..908110hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761058
Samples
Known GenesSUN1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442814
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