A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063328



Internal ID19152547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18685360..18709557hg38UCSC Ensembl
Innerchr21:20057678..20081875hg19UCSC Ensembl
Innerchr21:18979549..19003746hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3824198
hg1924198
hg1824198
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599811, nssv3599810, nssv3732670, nssv3599808, nssv3599812, nssv3599809
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)nsv1063328
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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