A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064577



Internal ID18807108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10338676..10582038hg38UCSC Ensembl
Innerchr21:10930419..11173781hg19UCSC Ensembl
Innerchr21:9952290..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38243363
hg19243363
hg18243363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4358n100
Supporting Variantsnssv3585037, nssv3585038
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064577
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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