A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999192



Internal ID19158728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75458231..75757215hg38UCSC Ensembl
Innerchr3:75507382..75806366hg19UCSC Ensembl
Innerchr3:75590072..75889056hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38298985
hg19298985
hg18298985
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4790n100
Supporting Variantsnssv3733728
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)nsv999192
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer