A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014312



Internal ID19103533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34434857..34498011hg38UCSC Ensembl
Innerchr2:34659924..34723078hg19UCSC Ensembl
Innerchr2:34513428..34576582hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3863155
hg1963155
hg1863155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3757n100
Supporting Variantsnssv3580906
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)nsv1014312
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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