A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956736



Internal ID17305609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10475728..10476283hg38UCSC Ensembl
Outerchr21:11036174..11036729hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003298
SamplesBILGI_BIOE
Known GenesBAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956736
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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