A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057371



Internal ID18799902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10472887..10643715hg38UCSC Ensembl
Innerchr21:10868742..11039570hg19UCSC Ensembl
Innerchr21:9890613..10061441hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38170829
hg19170829
hg18170829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4356n100
Supporting Variantsnssv3585016
Samples
Known GenesBAGE2, 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)nsv1057371
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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