A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590641



Internal ID16378050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75179222..75273092hg38UCSC Ensembl
Innerchr3:75228373..75322243hg19UCSC Ensembl
Innerchr3:75311063..75404933hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3893871
hg1993871
hg1893871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152257
SamplesHGDP00160
Known GenesMIR4444-1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590641
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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