A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008502



Internal ID19097720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75458231..75738575hg38UCSC Ensembl
Innerchr3:75507382..75787726hg19UCSC Ensembl
Innerchr3:75590072..75870416hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38280345
hg19280345
hg18280345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4790n100
Supporting Variantsnssv3733727, nssv3733726
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)nsv1008502
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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