A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953357



Internal ID17302231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:34905004..34936103hg38UCSC Ensembl
Outerchr21:36277301..36308400hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3831100
hg1931100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000670
SamplesBILGI_BIOE
Known GenesRUNX1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953357
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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