A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003886



Internal ID19093104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99178854..99230458hg38UCSC Ensembl
Innerchr3:98897698..98949302hg19UCSC Ensembl
Innerchr3:100380388..100431992hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3851605
hg1951605
hg1851605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4822n100
Supporting Variantsnssv3735185
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003886
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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