A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955278



Internal ID17304151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:162353191..162367290hg38UCSC Ensembl
Outerchr2:163209701..163223800hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3814100
hg1914100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003059
SamplesBILGI_BIOE
Known GenesGCA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955278
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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