A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441111



Internal ID22107290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7918137..7918137hg38UCSC Ensembl
chr4:7919864..7919864hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761012
Samples
Known GenesAFAP1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441111
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