A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954302



Internal ID16956489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10419922..10422697hg38UCSC Ensembl
Outerchr21:11089760..11092535hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg382776
hg192776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003262
SamplesBILGI_BIOE
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954302
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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