A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3480037



Internal ID18722278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103839821..104027079hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg18187259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999292
Supporting Variants
Samples
Known GenesACTG1P4, AMY1A, AMY1B, AMY1C, AMY2A, AMY2B, LOC101928436, RNPC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3480037
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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