A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061462



Internal ID19150681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24278004..24413936hg38UCSC Ensembl
Innerchr19:24460806..24596738hg19UCSC Ensembl
Innerchr19:24252646..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38135933
hg19135933
hg18135933
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3489n100
Supporting Variantsnssv3570732, nssv3570723, nssv3570727, nssv3570729, nssv3570731, nssv3570725, nssv3570730, nssv3570726, nssv3570728, nssv3570724
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)nsv1061462
Frequency
Sample Size11257
Observed Gain8
Observed Loss2
Observed Complex0
Frequencyn/a


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