A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063850



Internal ID18806381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36109645..36230404hg38UCSC Ensembl
Innerchr21:37481943..37602702hg19UCSC Ensembl
Innerchr21:36403813..36524572hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38120760
hg19120760
hg18120760
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4427n100
Supporting Variantsnssv3600159
Samples
Known GenesCBR3, CBR3-AS1, DOPEY2, LOC100133286
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063850
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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