A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013709



Internal ID19102928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45106843..45126291hg38UCSC Ensembl
Innerchr2:45333982..45353430hg19UCSC Ensembl
Innerchr2:45187486..45206934hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3819449
hg1919449
hg1819449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3803n100
Supporting Variantsnssv3581611
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013709
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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