A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151874



Internal ID15875602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12594207..12764624hg38UCSC Ensembl
Innerchr3:12635706..12806123hg19UCSC Ensembl
Innerchr3:12610706..12781123hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38170418
hg19170418
hg18170418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589704
Supporting Variants
SamplesHGDP00707
Known GenesRAF1, TMEM40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151874
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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