A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045493



Internal ID19134712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121516816..121540100hg38UCSC Ensembl
Innerchr10:123276330..123299614hg19UCSC Ensembl
Innerchr10:123266320..123289604hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3823285
hg1923285
hg1823285
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv981n100
Supporting Variantsnssv3514171
Samples
Known GenesFGFR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045493
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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