A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002336



Internal ID19091553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34434857..34501617hg38UCSC Ensembl
Innerchr2:34659924..34726684hg19UCSC Ensembl
Innerchr2:34513428..34580188hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3866761
hg1966761
hg1866761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3757n100
Supporting Variantsnssv3580907
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)nsv1002336
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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