A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013113



Internal ID18755644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103556018..103682498hg38UCSC Ensembl
Innerchr1:104098640..104225120hg19UCSC Ensembl
Innerchr1:103900163..104026643hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38126481
hg19126481
hg18126481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv217n100
Supporting Variantsnssv3474623
Samples
Known GenesACTG1P4, AMY1A, AMY1B, AMY1C, AMY2A, AMY2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013113
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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