A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061961



Internal ID19151180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36148980..36248226hg38UCSC Ensembl
Innerchr21:37521278..37620524hg19UCSC Ensembl
Innerchr21:36443148..36542394hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3899247
hg1999247
hg1899247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4428n100
Supporting Variantsnssv3600188
Samples
Known GenesCBR3-AS1, DOPEY2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061961
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer