A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730388



Internal ID20506299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121584377..121584617hg38UCSC Ensembl
chr10:123343891..123344131hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261510
Samples
Known GenesFGFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730388
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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