A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035944



Internal ID19125163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121564448..121589148hg38UCSC Ensembl
Innerchr10:123323962..123348662hg19UCSC Ensembl
Innerchr10:123313952..123338652hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3824701
hg1924701
hg1824701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503184
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)nsv1035944
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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