A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626388



Internal ID15849921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114870550..114871254hg38UCSC Ensembl
Outerchr2:114870113..114881811hg38UCSC Ensembl
Innerchr2:115628127..115628831hg19UCSC Ensembl
Outerchr2:115627690..115639388hg19UCSC Ensembl
Innerchr2:115344597..115345301hg18UCSC Ensembl
Outerchr2:115344160..115355858hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3811699
hg1911699
hg1811699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511185
Supporting Variants
Samples1
Known GenesDPP10
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626388
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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