A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003851



Internal ID19093069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74078951..74128221hg38UCSC Ensembl
Innerchr3:74128102..74177372hg19UCSC Ensembl
Innerchr3:74210792..74260062hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3849271
hg1949271
hg1849271
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3594162
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)nsv1003851
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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