A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998082



Internal ID19157619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75390630..75774408hg38UCSC Ensembl
Innerchr3:75439781..75823559hg19UCSC Ensembl
Innerchr3:75522471..75906249hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38383779
hg19383779
hg18383779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4773n100
Supporting Variantsnssv3733696
Samples
Known GenesFAM86DP, FLJ20518, 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)nsv998082
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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