A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999292



Internal ID18812142
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 StatusM
Merged Variantsdgv213n100
Supporting Variantsnssv3480037
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)nsv999292
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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