A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174132



Internal ID15874054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14946397..15028616hg38UCSC Ensembl
Innerchr10:14988396..15070615hg19UCSC Ensembl
Innerchr10:15028402..15110621hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3882220
hg1982220
hg1882220
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550005
Supporting Variants
SamplesHGDP00464
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174132
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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