A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063327



Internal ID19152546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18683769..18708616hg38UCSC Ensembl
Innerchr21:20056087..20080934hg19UCSC Ensembl
Innerchr21:18977958..19002805hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3824848
hg1924848
hg1824848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599721, nssv3599715, nssv3599704, nssv3599716, nssv3599705, nssv3599707, nssv3599720, nssv3599711, nssv3599722, nssv3599714, nssv3599718, nssv3599710, nssv3732609, nssv3599712, nssv3732610, nssv3599709, nssv3599719, nssv3732612, nssv3732611, nssv3599717, nssv3599708, nssv3599706, nssv3599713, nssv3599703
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)nsv1063327
Frequency
Sample Size11257
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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