A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006352



Internal ID19095569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4132155..4271801hg38UCSC Ensembl
Innerchr3:4173839..4313485hg19UCSC Ensembl
Innerchr3:4148839..4288485hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38139647
hg19139647
hg18139647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4652n100
Supporting Variantsnssv3591606, nssv3739579, nssv3591611, nssv3590493, nssv3591608, nssv3591602, nssv3591615, nssv3591607, nssv3590492, nssv3590494, nssv3591612, nssv3590491, nssv3591616, nssv3739578, nssv3591604, nssv3591609, nssv3591613, nssv3591614, nssv3591605, nssv3591610, nssv3591603
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)nsv1006352
Frequency
Sample Size11257
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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