A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003361



Internal ID19092580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34521378..34977235hg38UCSC Ensembl
Innerchr2:34746445..35202302hg19UCSC Ensembl
Innerchr2:34599949..35055806hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38455858
hg19455858
hg18455858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581119
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)nsv1003361
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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