A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039943



Internal ID19129162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121513508..121552365hg38UCSC Ensembl
Innerchr10:123273022..123311879hg19UCSC Ensembl
Innerchr10:123263012..123301869hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3838858
hg1938858
hg1838858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510484
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)nsv1039943
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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