A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518981



Internal ID18817262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121517335..121543133hg38UCSC Ensembl
Innerchr10:123276849..123302647hg19UCSC Ensembl
Innerchr10:123266839..123292637hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3825799
hg1925799
hg1825799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052154
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)nssv3518981
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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