A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099079



Internal ID22008312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121584386..121584386hg38UCSC Ensembl
chr10:123343900..123343900hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587148
Samples
Known GenesFGFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099079
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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