A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062721



Internal ID19151940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27390266hg38UCSC Ensembl
Innerchr19:27747981..27881174hg19UCSC Ensembl
Innerchr19:32439821..32573014hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38133194
hg19133194
hg18133194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3494n100
Supporting Variantsnssv3570803, nssv3570809, nssv3570816, nssv3570817, nssv3570823, nssv3570821, nssv3570818, nssv3570807, nssv3570813, nssv3570820, nssv3570811, nssv3570808, nssv3570805, nssv3570822, nssv3570804, nssv3570810, nssv3570819, nssv3570801, nssv3570806, nssv3570814, nssv3570815, nssv3570802, nssv3570812
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)nsv1062721
Frequency
Sample Size11257
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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