A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv916121



Internal ID16210077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114870113..114871217hg38UCSC Ensembl
Innerchr2:115627690..115628794hg19UCSC Ensembl
Innerchr2:115344160..115345264hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381105
hg191105
hg181105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582728
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)nssv916121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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