A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064468



Internal ID18806999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10448879..10643715hg38UCSC Ensembl
Innerchr21:10868742..11063578hg19UCSC Ensembl
Innerchr21:9890613..10085449hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38194837
hg19194837
hg18194837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4356n100
Supporting Variantsnssv3732531
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)nsv1064468
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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