A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444501



Internal ID22110681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121584336..121584336hg38UCSC Ensembl
chr10:123343850..123343850hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760776
Samples
Known GenesFGFR2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444501
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