A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065276



Internal ID18807807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10420787..10576547hg38UCSC Ensembl
Innerchr21:10935910..11091670hg19UCSC Ensembl
Innerchr21:9957781..10113541hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38155761
hg19155761
hg18155761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4363n100
Supporting Variantsnssv3585049
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)nsv1065276
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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