A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955276



Internal ID16957463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:161136390..161145289hg38UCSC Ensembl
Outerchr2:161992901..162001800hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003057
SamplesBILGI_BIOE
Known GenesTANK
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955276
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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