A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153417



Internal ID15531029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192716269..192885540hg38UCSC Ensembl
Innerchr3:192434058..192603329hg19UCSC Ensembl
Innerchr3:193916752..194086023hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38169272
hg19169272
hg18169272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592905
Supporting Variants
SamplesHGDP01033
Known GenesFGF12, MB21D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153417
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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