A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv916285



Internal ID16210241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:115043032..115077076hg38UCSC Ensembl
Innerchr2:115800609..115834653hg19UCSC Ensembl
Innerchr2:115517079..115551123hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3834045
hg1934045
hg1834045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582732
Supporting Variants
Samples
Known GenesDPP10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv916285
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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