A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004196



Internal ID19093413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26547361..26580527hg38UCSC Ensembl
Innerchr3:26588852..26622018hg19UCSC Ensembl
Innerchr3:26563856..26597022hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3833167
hg1933167
hg1833167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589559
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)nsv1004196
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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