A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055301



Internal ID18797832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10404321..10524598hg38UCSC Ensembl
Innerchr21:10987859..11108136hg19UCSC Ensembl
Innerchr21:10009730..10130007hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38120278
hg19120278
hg18120278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4370n100
Supporting Variantsnssv3585111
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)nsv1055301
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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