A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010147



Internal ID19099366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75497567..75738954hg38UCSC Ensembl
Innerchr3:75546718..75788105hg19UCSC Ensembl
Innerchr3:75629408..75870795hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38241388
hg19241388
hg18241388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4790n100
Supporting Variantsnssv3733755
Samples
Known GenesFLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010147
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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