A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514171



Internal ID18812452
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 StatusS
Merged Variantsnsv1045493
Supporting Variants
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)nssv3514171
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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