A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv874296



Internal ID6281307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:75030680..75128176hg19UCSC Ensembl
Outerchr2:75012327..75138538hg19UCSC Ensembl
Innerchr2:74884188..74981684hg18UCSC Ensembl
Outerchr2:74865835..74992046hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1552935
SamplesMS19649
Known GenesHK2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv874296
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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