A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150490



Internal ID15529426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:114737565..114815922hg38UCSC Ensembl
Innerchr2:115495142..115573499hg19UCSC Ensembl
Innerchr2:115211612..115289969hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3878358
hg1978358
hg1878358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582715
Supporting Variants
SamplesHGDP00786
Known GenesDPP10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150490
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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